Novel methods of diagnosis of metastatic colorectal cancer, compositions and methods of screening for modulators of metastatic colorectal cancer

ABSTRACT

Described herein are methods and compositions that can be used for diagnosis and treatment of metastatic colorectal cancer. Also described herein are methods that can be used to identify modulators of metastatic colorectal cancer.

CROSS-REFERENCES TO RELATED APPLICATIONS

[0001] The present application is related to U.S. S No. 60/272,206, filed Feb. 27, 2001, U.S. S No. 60/281,149, filed Apr. 2, 2001, and U.S. S No. 60/284,555, filed Apr. 17, 2001, all of which are herein incorporated by referenced in their entirety.

FIELD OF THE INVENTION

[0002] The invention relates to the identification of nucleic acid and protein expression profiles and nucleic acids, products, and antibodies thereto that are involved in metastatic colorectal cancer; and to the use of such expression profiles and compositions in diagnosis and therapy of metastatic colorectal cancer. The invention further relates to methods for identifying and using agents and/or targets that inhibit metastatic colorectal cancer.

BACKGROUND OF THE INVENTION

[0003] Cancer of the colon and/or rectum (referred to as “colorectal cancer”) are significant in Western populations and particularly in the United States. Cancers of the colon and rectum occur in both men and women most commonly after the age of 50. These develop as the result of a pathologic transformation of normal colon epithelium to an invasive cancer. There have been a number of recently characterized genetic alterations that have been implicated in colorectal cancer, including mutations in two classes of genes, tumor-suppressor genes and proto-oncogenes, with recent work suggesting that mutations in DNA repair genes may also be involved in tumorigenesis. For example, inactivating mutations of both alleles of the adenomatous polyposis coli (APC) gene, a tumor suppressor gene, appears to be one of the earliest events in colorectal cancer, and may even be the initiating event. Other genes implicated in colorectal cancer include the MCC gene, the p53 gene, the DCC (deleted in colorectal carcinoma) gene and other chromosome 18q genes, and genes in the TGF-β signaling pathway. For a review, see Molecular Biology of Colorectal Cancer, pp. 238-299, in Curr. Probl. Cancer, September/October 1997; see also Willams, Colorectal Cancer (1996); Kinsella & Schofield, Colorectal Cancer: A Scientific Perspective (1993); Colorectal Cancer: Molecular Mechanisms, Premalignant State and its Prevention (Schiniegel & Scholmerich eds., 2000); Colorectal Cancer: New Aspects of molecular Biology and Their Clinical Applications (Hanski et al., eds 2000); McArdle et al., Colorectal Cancer (2000); Wanebo, Colorectal Cancer (1993); Levin, The American Cancer Society: Colorectal Cancer (1999); Treatment of Hepatic Metastases of Colorectal Cancer (Nordlinger & Jaeck eds., 1993); Management of Colorectal Cancer (Dunitz et al., eds. 1998); Cancer: Principles and Practice of Oncology (Devita et al., eds. 2001); Surgical Oncology: Contemporary Principles and Practice (Kirby et al., eds. 2001); Offit, Clinical Cancer Genetics: Risk Counseling and Management (1997); Radioimmunotherapy of Cancer (Abrams & Fritzberg eds. 2000); Fleming, AJCC Cancer Staging Handbook (1998); Textbook of Radiation Oncology (Leibel & Phillips eds. 2000); and Clinical Oncology (Abeloff et al., eds. 2000).

[0004] Imaging of colorectal cancer for diagnosis has been problematic and limited.

[0005] In addition, metastasis of the tumor to the lumen, and metastasis of tumor cells to regional lymph nodes are important prognostic factors (see, e.g., PET in Oncology: Basics and Clinical Application (Ruhlmann et al. eds. 1999). For example, five year survival rates drop from 80 percent in patients with no lymph node metastases to 45 to 50 percent in those patients who do have lymph node metastases. A recent report showed that micrometastases can be detected from lymph nodes using reverse transcriptase-PCR methods based on the presence of mRNA for carcinoembryonic antigen, which has previously been shown to be present in the vast majority of colorectal cancers but not in normal tissues. Liefers et al., New England J. of Med. 339(4):223 (1998). In addition, colorectal cancers often metastasize to the liver. However, the lack of information about the gene expression exhibited by these cancers limits the ability to effectively diagnose and treat the disease. Thus, methods for diagnosis and prognosis of metastatic colorectal cancer and effective treatment of colorectal cancer would be desirable. Accordingly, provided herein are methods that can be used in diagnosis and prognosis of metastatic colorectal cancer. Further provided are methods that can be used to screen candidate therapeutic agents for the ability to modulate, e.g., treat, colorectal cancer. Additionally, provided herein are molecular targets and compositions for therapeutic intervention in metastatic colorectal disease and other metastatic cancers.

SUMMARY OF THE INVENTION

[0006] The present invention therefore provides nueleotide sequences of genes that are up- and down-regulated in metastatic colorectal cancer cells. Such genes and the proteins they encode are useful for diagnostic and prognostic purposes, and also as targets for screening for therapeutic compounds that modulate metastatic colorectal cancer, such as antibodies. The methods of detecting nucleic acids of the invention or their encoded proteins can be used for a number of purposes. Examples include, early detection of colon cancers, monitoring and early detection of relapse following treatment of colon cancers, monitoring response to therapy of colon cancers, determining prognosis of colon cancers, directing therapy of colon cancers, selecting patients for postoperative chemotherapy or radiation therapy, selecting therapy, determining tumor prognosis, treatment, or response to treatment, and early detection of precancerous colon adenomas. Other aspects of the invention will become apparent to the skilled artisan by the following description of the invention.

[0007] In one aspect, the present invention provides a method of detecting a metastatic colorectal cancer-associated transcript in a cell from a patient, the method comprising contacting a biological sample from the patient with a polynucleotide that selectively hybridizes to a sequence at least 80% identical to a sequence as shown in Tables 1-26.

[0008] In one embodiment, the polynucleotide selectively hybridizes to a sequence at least 95% identical to a sequence as shown in Tables 1-26. In another embodiment, the polynucleotide comprises a sequence as shown in Tables 1-26.

[0009] In one embodiment, the biological sample is a tissue sample. In another embodiment, the biological sample comprises isolated nucleic acids, e.g., mRNA.

[0010] In one embodiment, the polynucleotide is labeled, e.g., with a fluorescent label.

[0011] In one embodiment, the polynucleotide is immobilized on a solid surface.

[0012] In one embodiment, the patient is undergoing a therapeutic regimen to treat metastatic colorectal cancer. In another embodiment, the patient is suspected of having metastatic colorectal cancer.

[0013] In one embodiment, the patient is a human.

[0014] In one embodiment, the method further comprises the step of amplifying nucleic acids before the step of contacting the biological sample with the polynucleotide.

[0015] In another aspect, the present invention provides methods of detecting polypeptide encoded by a metastatic colorectal cancer-associated transcript in a cell from a patient, the method comprising contacting a biological sample from the patient with an antibody that specifically binds a polypeptide encoded by a sequence at least 80% identical to a sequence as shown in Tables 1-26.

[0016] In another aspect, the present invention provides a method of monitoring the efficacy of a therapeutic treatment of metastatic colorectal cancer, the method comprising the steps of: (i) providing a biological sample from a patient undergoing the therapeutic treatment; and (ii) determining the level of a metastatic colorectal cancer-associated transcript in the biological sample by contacting the biological sample with a polynucleotide that selectively hybridizes to a sequence at least 80% identical to a sequence as shown in Tables 1-26., thereby monitoring the efficacy of the therapy.

[0017] In one embodiment, the method further comprises the step of: (iii) comparing the level of the metastatic colorectal cancer-associated transcript to a level of the metastatic colorectal cancer-associated transcript in a biological sample from the patient prior to, or earlier in, the therapeutic treatment.

[0018] In another aspect, the present invention provides a method of monitoring the efficacy of a therapeutic treatment of metastatic colorectal cancer, the method comprising the steps of: (i) providing a biological sample from a patient undergoing the therapeutic treatment; and (ii) determining the level of a metastatic colorectal cancer-associated antibody in the biological sample by contacting the biological sample with a polypeptide encoded by a polynucleotide that selectively hybridizes to a sequence at least 80% identical to a sequence as shown in Tables 1-26, wherein the polypeptide specifically binds to the metastatic colorectal cancer-associated antibody, thereby monitoring the efficacy of the therapy.

[0019] In one embodiment, the method further comprises the step of: (iii) comparing the level of the metastatic colorectal cancer-associated antibody to a level of the metastatic colorectal cancer-associated antibody in a biological sample from the patient prior to, or earlier in, the therapeutic treatment.

[0020] In another aspect, the present invention provides a method of monitoring the efficacy of a therapeutic treatment of metastatic colorectal cancer, the method comprising the steps of: (i) providing a biological sample from a patient undergoing the therapeutic treatment; and (ii) determining the level of a metastatic colorectal cancer-associated polypeptide in the biological sample by contacting the biological sample with an antibody, wherein the antibody specifically binds to a polypeptide encoded by a polynucleotide that selectively hybridizes to a sequence at least 80% identical to a sequence as shown in Tables 1-26, thereby monitoring the efficacy of the therapy.

[0021] In one embodiment, the method further comprises the step of: (iii) comparing the level of the metastatic colorectal cancer-associated polypeptide to a level of the metastatic colorectal cancer-associated polypeptide in a biological sample from the patient prior to, or earlier in, the therapeutic treatment.

[0022] In one aspect, the present invention provides an isolated nucleic acid molecule consisting of a polynucleotide sequence as shown in Tables 1-26.

[0023] In one embodiment, an expression vector or cell comprises the isolated nucleic acid.

[0024] In one aspect, the present invention provides an isolated polypeptide which is encoded by a nucleic acid molecule having polynucleotide sequence as shown in Tables 1-26.

[0025] In another aspect, the present invention provides an antibody that specifically binds to an isolated polypeptide which is encoded by a nucleic acid molecule having polynucleotide sequence as shown in Tables 1-26.

[0026] In one embodiment, the antibody is conjugated to an effector component, e.g., a fluorescent label, a radioisotope or a cytotoxic chemical.

[0027] In one embodiment, the antibody is an antibody fragment. In another embodiment, the antibody is humanized.

[0028] In one aspect, the present invention provides a method of detecting a metastatic colorectal cancer cell in a biological sample from a patient, the method comprising contacting the biological sample with an antibody as described herein.

[0029] In another aspect, the present invention provides a method of detecting antibodies specific to metastatic colorectal cancer in a patient, the method comprising contacting a biological sample from the patient with a polypeptide encoded by a nucleic acid comprises a sequence from Tables 1-26.

[0030] In another aspect, the present invention provides a method for identifying a compound that modulates a metastatic colorectal cancer-associated polypeptide, the method comprising the steps of: (i) contacting the compound with a metastatic colorectal cancer-associated polypeptide, the polypeptide encoded by a polynucleotide that selectively hybridizes to a sequence at least 80% identical to a sequence as shown in Tables 1-26; and (ii) determining the functional effect of the compound upon the polypeptide.

[0031] In one embodiment, the functional effect is a physical effect, an enzymatic effect, or a chemical effect.

[0032] In one embodiment, the polypeptide is expressed in a eukaryotic host cell or cell membrane. In another embodiment, the polypeptide is recombinant.

[0033] In one embodiment, the functional effect is determined by measuring ligand binding to the polypeptide.

[0034] In another aspect, the present invention provides a method of inhibiting proliferation of a metastatic colorectal cancer-associated cell to treat colorectal cancer in a patient, the method comprising the step of administering to the subject a therapeutically effective amount of a compound identified as described herein.

[0035] In one embodiment, the compound is an antibody.

[0036] In another aspect, the present invention provides a drug screening assay comprising the steps of: (i) administering a test compound to a mammal having colorectal cancer or a cell isolated therefrom; (ii) comparing the level of gene expression of a polynucleotide that selectively hybridizes to a sequence at least 80% identical to a sequence as shown in Tables 1-26. in a treated cell or mammal with the level of gene expression of the polynucleotide in a control cell or mammal, wherein a test compound that modulates the level of expression of the polynucleotide is a candidate for the treatment of colorectal cancer.

[0037] In one embodiment, the control is a mammal with colorectal cancer or a cell therefrom that has not been treated with the test compound. In another embodiment, the control is a normal cell or mammal.

[0038] In another aspect, the present invention provides a method for treating a mammal having colorectal cancer comprising administering a compound identified by the assay described herein.

[0039] In another aspect, the present invention provides a pharmaceutical composition for treating a mammal having colorectal cancer, the composition comprising a compound identified by the assay described herein and a physiologically acceptable excipient.

DETAILED DESCRIPTION OF THE INVENTION

[0040] In accordance with the objects outlined above, the present invention provides novel methods for diagnosis and treatment of colon and/or rectal cancer (e.g. colorectal cancer), including metastatic colorectal cancers, as well as methods for screening for compositions which modulate colorectal cancer. By “metastatic colorectal cancer” herein is meant a colon and/or rectal tumor or cancer that is classified as Dukes stage C or D (see, e.g., Cohen et al., Cancer of the Colon, in Cancer: Principles and Practice of Oncology, pp. 1144-1197 (Devita et al., eds., 5^(th) ed. 1997); see also Harrison 's Principles of Internal Medicine, pp. 1289-129 (Wilson et al., eds., 12^(th) ed., 1991). “Treatment, monitoring, detection or modulation of metastatic colorectal cancer” includes treatment, monitoring, detection, or modulation of metastatic colorectal disease in those patients who have metastatic colorectal disease (Dukes stage C or D). In Dukes stage A, the tumor has penetrated into, but not through, the bowel wall. In Dukes stage B, the tumor has penetrated through the bowel wall but there is not yet any lymph involvement. In Dukes stage C, the cancer involves regional lymph nodes. In Dukes stage D, there is distant metastasis, e.g., liver, lung, etc.

[0041] Tables 1-26 provide UniGene cluster identification numbers for the nucleotide sequence of genes that exhibit increased or decreased expression in metastasizing colorectal cancer samples. Tables 1-26 also provide an exemplar accession number that provides a nucleotide sequence that is part of the UniGene cluster. In Tables 1-26, the ratio provided represents primary tumor samples from known Dukes B stage survivors vs. liver metastasis samples from patients with metastatic colorectal cancer. In these samples, the identified genes are underexpressed in the metastatic samples, as the ratio is greater than one, preferably 1.5 or greater, more preferably 2.0 or greater. In Tables 1-26, the ratio provided represents liver metastasis samples from patients with known metastatic colorectal cancer vs. known primary tumor samples from Dukes B stage survivors. In these samples, the identified genes are overexpressed in the metastatic samples, as the ratio is greater than one, preferably 1.5 or greater, more preferably 2.0 or greater. In Tables 1-26, the ratio provided represents primary tumor samples from known Dukes B stage survivors vs. liver metastasis samples from patients with metastatic colorectal cancer. In these samples, the identified genes are overexpressed in the metastatic samples, as the ratio is less than one, preferably 0.5 or less, more preferably 0.25 or less. Survivors are subjects who have been disease free for five years or longer.

[0042] In Tables 1-26, the ratio provided represents liver metastasis samples from patients with known metastatic disease vs. tissue samples from normal colon tissue. In these samples, the identified genes are overexpressed in the metastatic samples, as the ratio is greater than one, preferably 1.5 or greater, more preferably 2.0 or greater. In Tables 1-26, the ratio represents liver metastasis samples from patients with known metastatic disease vs. tissue samples from normal colon tissue. In these samples, the identified genes are underexpressed in the metastatic samples, as the ratio is less than one, preferably 0.5 or less, more preferably 0.25 or less.

[0043] One of skill will recognize that although the sequences identified in Tables 1-26 exhibited increased or decreased expression in metastasizing colorectal cancer samples, the sequences of the invention, and their encoded proteins, can be used to diagnose, treat or prevent cancers in patients with Dukes stage A or B colorectal cancers. Alteration of gene expression for a gene in Tables 1-26 may be more likely or less likely to indicate that the subject will progress to metastatic disease. The sequences can also be used to diagnose, treat or prevent precancerous or benign conditions such as precancerous colon adenomas. Alteration of gene expression for a gene in Tables 1-26 may or may not indicate that the subject is more likely to progress to cancer or to metastatic disease. Thus, although the specification focuses primarily on metastasizing colorectal cancer, the methods described below can also be applied to non-metastasizing colorectal cancers (e.g., Dukes stages A and B) and precancerous or benign conditions (e.g., precancerous adenomas) as well.

[0044] Definitions

[0045] The term “metastatic colorectal cancer protein” or “metastatic colorectal cancer polynucleotide” or “metastatic colorectal cancer-associated transcript” refers to nucleic acid and polypeptide polymorphic variants, alleles, mutants, and interspecies homologs that: (1) have a nucleotide sequence that has greater than about 60% nucleotide sequence identity, 65%, 70%, 75%, 80%, 85%, 90%, preferably 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99% or greater nucleotide sequence identity, preferably over a region of over a region of at least about 25, 50, 100, 200, 500, 1000, or more nucleotides, to a nucleotide sequence of or associated with a UniGene cluster of Tables 1-26; (2) bind to antibodies, e.g., polyclonal antibodies, raised against an immunogen comprising an amino acid sequence encoded by a nucleotide sequence of or associated with a UniGene cluster of Tables 1-26, and conservatively modified variants thereof; (3) specifically hybridize under stringent hybridization conditions to a nucleic acid sequence, or the complement thereof of Tables 1-26 and conservatively modified variants thereof or (4) have an amino acid sequence that has greater than about 60% amino acid sequence identity, 65%, 70%, 75%, 80%, 85%, 90%, preferably 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99% or greater amino sequence identity, preferably over a region of over a region of at least about 25, 50, 100, 200, 500, 1000, or more amino acid, to an amino acid sequence encoded by a nucleotide sequence of or associated with a UniGene cluster of Tables 1-26. A polynucleotide or polypeptide sequence is typically from a mammal including, but not limited to, primate, e.g., human; rodent, e.g., rat, mouse, hamster; cow, pig, horse, sheep, or other mammal. A “metastatic colorectal cancer polypeptide” and a “metastatic colorectal cancer polynucleotide,” include both naturally occurring or recombinant.

[0046] A “fill length” metastatic colorectal cancer protein or nucleic acid refers to a metastatic colorectal cancer polypeptide or polynucleotide sequence, or a variant thereof, that contains all of the elements normally contained in one or more naturally occurring, wild type metastatic colorectal cancer polynucleotide or polypeptide sequences. The “full length” may be prior to, or after, various stages of post-translation processing or splicing, including alternative splicing.

[0047] “Biological sample” as used herein is a sample of biological tissue or fluid that contains nucleic acids or polypeptides, e.g., of a metastatic colorectal cancer protein, polynucleotide or transcript. Such samples include, but are not limited to, tissue isolated from primates, e.g., humans, or rodents, e.g., mice, and rats. Biological samples may also include sections of tissues such as biopsy and autopsy samples, frozen sections taken for histologic purposes, blood, plasma, serum, sputum, stool, tears, mucus, hair, skin, etc. Biological samples also include explants and primary and/or transformed cell cultures derived from patient tissues. A biological sample is typically obtained from a eukaryotic organism, most preferably a mammal such as a primate, e.g., chimpanzee or human; cow; dog; cat; a rodent, e.g., guinea pig, rat, mouse; rabbit; or other mammal; or a bird; reptile; fish.

[0048] “Providing a biological sample” means to obtain a biological sample for use in methods described in this invention. Most often, this will be done by removing a sample of cells from an animal, but can also be accomplished by using previously isolated cells (e.g., isolated by another person, at another time, and/or for another purpose), or by performing the methods of the invention in vivo. Archival tissues, having treatment or outcome history, will be particularly useful.

[0049] The terms “identical” or percent “identity,” in the context of two or more nucleic acids or polypeptide sequences, refer to two or more sequences or subsequences that are the same or have a specified percentage of amino acid residues or nucleotides that are the same (i.e., about 60% identity, preferably 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or higher identity over a specified region, when compared and aligned for maximum correspondence over a comparison window or designated region) as measured using a BLAST or BLAST 2.0 sequence comparison algorithms with default parameters described below, or by manual alignment and visual inspection (see, e.g. NCBI web site http://www.ncbi.nlm.nih.gov/BLAST/ or the like). Such sequences are then said to be “substantially identical.” This definition also refers to, or may be applied to, the compliment of a test sequence. The definition also includes sequences that have deletions and/or additions, as well as those that have substitutions, as well as naturally occurring, e.g., polymorphic or allelic variants, and man-made variants. As described below, the preferred algorithms can account for gaps and the like. Preferably, identity exists over a region that is at least about 25 amino acids or nucleotides in length, or more preferably over a region that is 50-100 amino acids or nucleotides in length.

[0050] For sequence comparison, typically one sequence acts as a reference sequence, to which test sequences are compared. When using a sequence comparison algorithm, test and reference sequences are entered into a computer, subsequence coordinates are designated, if necessary, and sequence algorithm program parameters are designated. Preferably, default program parameters can be used, or alternative parameters can be designated. The sequence comparison algorithm then calculates the percent sequence identities for the test sequences relative to the reference sequence, based on the program parameters.

[0051] A “comparison window”, as used herein, includes reference to a segment of one of the number of contiguous positions selected from the group consisting typically of from 20 to 600, usually about 50 to about 200, more usually about 100 to about 150 in which a sequence may be compared to a reference sequence of the same number of contiguous positions after the two sequences are optimally aligned. Methods of alignment of sequences for comparison are well-known in the art. Optimal alignment of sequences for comparison can be conducted, e.g., by the local homology algorithm of Smith & Waterman, Adv. Appl. Math. 2:482 (1981), by the homology alignment algorithm of Needleman & Wunsch, J. Mol. Biol. 48:443 (1970), by the search for similarity method of Pearson & Lipman, Proc. Nat'l. Acad. Sci. USA 85:2444 (1988), by computerized implementations of these algorithms (GAP, BESTFIT, FASTA, and TFASTA in the Wisconsin Genetics Software Package, Genetics Computer Group, 575 Science Dr., Madison, Wis.), or by manual alignment and visual inspection (see, e.g., Current Protocols in Molecular Biology (Ausubel et al., eds. 1995 supplement)).

[0052] Preferred examples of algorithms that are suitable for determining percent sequence identity and sequence similarity include the BLAST and BLAST 2.0 algorithms, which are described in Altschul et al., Nuc. Acids Res. 25:3389-3402 (1977) and Altschul et al., J. Mol. Biol. 215:403-410 (1990). BLAST and BLAST 2.0 are used, with the parameters described herein, to determine percent sequence identity for the nucleic acids and proteins of the invention. Software for performing BLAST analyses is publicly available through the National Center for Biotechnology Information (http://www.ncbi.nlm.nih.gov/). This algorithm involves first identifying high scoring sequence pairs (HSPs) by identifying short words of length W in the query sequence, which either match or satisfy some positive-valued threshold score T when aligned with a word of the same length in a database sequence. T is referred to as the neighborhood word score threshold (Altschul et al., supra). These initial neighborhood word hits act as seeds for initiating searches to find longer HSPs containing them. The word hits are extended in both directions along each sequence for as far as the cumulative alignment score can be increased. Cumulative scores are calculated using, e.g., for nucleotide sequences, the parameters M (reward score for a pair of matching residues; always >0) and N (penalty score for mismatching residues; always <0). For amino acid sequences, a scoring matrix is used to calculate the cumulative score. Extension of the word hits in each direction are halted when: the cumulative alignment score falls off by the quantity X from its maximum achieved value; the cumulative score goes to zero or below, due to the accumulation of one or more negative-scoring residue alignments; or the end of either sequence is reached. The BLAST algorithm parameters W, T, and X determine the sensitivity and speed of the alignment. The BLASTN program (for nucleotide sequences) uses as defaults a wordlength (W) of 11, an expectation (E) of 10, M=5, N=−4 and a comparison of both strands. For amino acid sequences, the BLASTP program uses as defaults a wordlength of 3, and expectation (E) of 10, and the BLOSUM62 scoring matrix (see Henikoff& Henikoff, Proc. Natl. Acad. Sci. USA 89:10915 (1989)) alignments (B) of 50, expectation (E) of 10, M=5, N=−4, and a comparison of both strands.

[0053] The BLAST algorithm also performs a statistical analysis of the similarity between two sequences (see, e.g., Karlin & Altschul, Proc. Nat'l. Acad. Sci. USA 90:5873-5787 (1993)). One measure of similarity provided by the BLAST algorithm is the smallest sum probability (P(N)), which provides an indication of the probability by which a match between two nucleotide or amino acid sequences would occur by chance. For example, a nucleic acid is considered similar to a reference sequence if the smallest sum probability in a comparison of the test nucleic acid to the reference nucleic acid is less than about 0.2, more preferably less than about 0.01, and most preferably less than about 0.001. Log values may be large negative numbers, e.g., 5, 10, 20, 30, 40, 40, 70, 90, 110, 150, 170, etc.

[0054] An indication that two nucleic acid sequences or polypeptides are substantially identical is that the polypeptide encoded by the first nucleic acid is immunologically cross reactive with the antibodies raised against the polypeptide encoded by the second nucleic acid, as described below. Thus, a polypeptide is typically substantially identical to a second polypeptide, e.g., where the two peptides differ only by conservative substitutions. Another indication that two nucleic acid sequences are substantially identical is that the two molecules or their complements hybridize to each other under stringent conditions, as described below. Yet another indication that two nucleic acid sequences are substantially identical is that the same primers can be used to amplify the sequences.

[0055] A “host cell” is a naturally occurring cell or a transformed cell that contains an expression vector and supports the replication or expression of the expression vector. Host cells may be cultured cells, explants, cells in vivo, and the like. Host cells may be prokaryotic cells such as E. coli, or eukaryotic cells such as yeast, insect, amphibian, or mammalian cells such as CHO, HeLa, and the like (see, e.g., the American Type Culture Collection catalog or web site, www.atcc.org).

[0056] The terms “isolated,” “purified,” or “biologically pure” refer to material that is substantially or essentially free from components that normally accompany it as found in its native state. Purity and homogeneity are typically determined using analytical chemistry techniques such as polyacrylamide gel electrophoresis or high performance liquid chromatography. A protein or nucleic acid that is the predominant species present in a preparation is substantially purified. In particular, an isolated nucleic acid is separated from some open reading frames that naturally flank the gene and encode proteins other than protein encoded by the gene. The term “purified” in some embodiments denotes that a nucleic acid or protein gives rise to essentially one band in an electrophoretic gel. Preferably, it means that the nucleic acid or protein is at least 85% pure, more preferably at least 95% pure, and most preferably at least 99% pure. “Purify” or “purification” in other embodiments means removing at least one contaminant from the composition to be purified. In this sense, purification does not require that the purified compound be homogenous, e.g., 100% pure.

[0057] The terms “polypeptide,” “peptide” and “protein” are used interchangeably herein to refer to a polymer of amino acid residues. The terms apply to amino acid polymers in which one or more amino acid residue is an artificial chemical mimetic of a corresponding naturally occurring amino acid, as well as to naturally occurring amino acid polymers, those containing modified residues, and non-naturally occurring amino acid polymer.

[0058] The term “amino acid” refers to naturally occurring and synthetic amino acids, as well as amino acid analogs and amino acid mimetics that function similarly to the naturally occurring amino acids. Naturally occurring amino acids are those encoded by the genetic code, as well as those amino acids that are later modified, e.g., hydroxyproline, γ-carboxyglutamate, and O-phosphoserine. Amino acid analogs refers to compounds that have the same basic chemical structure as a naturally occurring amino acid, e.g., an a carbon that is bound to a hydrogen, a carboxyl group, an amino group, and an R group, e.g., homoserine, norleucine, methionine sulfoxide, methionine methyl sulfonium. Such analogs may have modified R groups (e.g., norleucine) or modified peptide backbones, but retain the same basic chemical structure as a naturally occurring amino acid. Amino acid mimetics refers to chemical compounds that have a structure that is different from the general chemical structure of an amino acid, but that functions similarly to a naturally occurring amino acid.

[0059] Amino acids may be referred to herein by either their commonly known three letter symbols or by the one-letter symbols recommended by the IUPAC-IUB Biochemical Nomenclature Commission. Nucleotides, likewise, may be referred to by their commonly accepted single-letter codes.

[0060] “Conservatively modified variants” applies to both amino acid and nucleic acid sequences. With respect to particular nucleic acid sequences, conservatively modified variants refers to those nucleic acids which encode identical or essentially identical amino acid sequences, or where the nucleic acid does not encode an amino acid sequence, to essentially identical or associated, e.g., naturally contiguous, sequences. Because of the degeneracy of the genetic code, a large number of functionally identical nucleic acids encode most proteins. For instance, the codons GCA, GCC, GCG and GCU all encode the amino acid alanine. Thus, at every position where an alanine is specified by a codon, the codon can be altered to another of the corresponding codons described without altering the encoded polypeptide. Such nucleic acid variations are “silent variations,” which are one species of conservatively modified variations. Every nucleic acid sequence herein which encodes a polypeptide also describes silent variations of the nucleic acid. One of skill will recognize that in certain contexts each codon in a nucleic acid (except AUG, which is ordinarily the only codon for methionine, and TGG, which is ordinarily the only codon for tryptophan) can be modified to yield a functionally identical molecule. Accordingly, often silent variations of a nucleic acid which encodes a polypeptide is implicit in a described sequence with respect to the expression product, but not with respect to actual probe sequences.

[0061] As to amino acid sequences, one of skill will recognize that individual substitutions, deletions or additions to a nucleic acid, peptide, polypeptide, or protein sequence which alters, adds or deletes a single amino acid or a small percentage of amino acids in the encoded sequence is a “conservatively modified variant” where the alteration results in the substitution of an amino acid with a chemically similar amino acid. Conservative substitution tables providing functionally similar amino acids are well known in the art. Such conservatively modified variants are in addition to and do not exclude polymorphic variants, interspecies homologs, and alleles of the invention.

[0062] The following eight groups each contain amino acids that are typically conservative substitutions for one another: 1) Alanine (A), Glycine (G); 2) Aspartic acid (D), Glutamic acid (E); 3) Asparagine (N), Glutamine (O); 4) Arginine (R), Lysine (K); 5) Isoleucine (I), Leucine (L), Methionine (M), Valine (V); 6) Phenylalanine (F), Tyrosine (Y), Tryptophan (W); 7) Serine (S), Threonine (T); and 8) Cysteine (C), Methionine (M) (see, e.g., Creighton, Proteins (1984)).

[0063] Macromolecular structures such as polypeptide structures can be described in terms of various levels of organization. For a general discussion of this organization, see, e.g., Alberts et al., Molecular Biology of the Cell (3^(rd) ed., 1994) and Cantor & Schimmel, Biophysical Chemistry Part I. The Conformation of Biological Macromolecules (1980). “Primary structure” refers to the amino acid sequence of a particular peptide. “Secondary structure” refers to locally ordered, three dimensional structures within a polypeptide. These structures are commonly known as domains. Domains are portions of a polypeptide that often form a compact unit of the polypeptide and are typically 25 to approximately 500 amino acids long. Typical domains are made up of sections of lesser organization such as stretches of β-sheet and α-helices. “Tertiary structure” refers to the complete three dimensional structure of a polypeptide monomer. “Quaternary structure” refers to the three dimensional structure formed, usually by the noncovalent association of independent tertiary units. Anisotropic terms are also known as energy terms.

[0064] “Nucleic acid” or “oligonucleotide” or “polynucleotide” or grammatical equivalents used herein means at least two nucleotides covalently linked together. Oligonucleotides are typically from about 5, 6, 7, 8, 9, 10, 12, 15, 25, 30, 40, 50 or more nucleotides in length, up to about 100 nucleotides in length. Nucleic acids and polynucleotides are a polymers of any length, including longer lengths, e.g., 200, 300, 500, 1000, 2000, 3000, 5000, 7000, 10,000, etc. A nucleic acid of the present invention will generally contain phosphodiester bonds, although in some cases, nucleic acid analogs are included that may have alternate backbones, comprising, e.g., phosphoramidate, phosphorothioate, phosphorodithioate, or O-methylphophoroamidite linkages (see Eckstein, Oligonucleotides and Analogues: A Practical Approach, Oxford University Press); and peptide nucleic acid backbones and linkages. Other analog nucleic acids include those with positive backbones; non-ionic backbones, and non-ribose backbones, including those described in U.S. Pat. Nos. 5,235,033 and 5,034,506, and Chapters 6 and 7, ASC Symposium Series 580, Carbohydrate Modifications in Antisense Research, Sanghui & Cook, eds. Nucleic acids containing one or more carbocyclic sugars are also included within one definition of nucleic acids. Modifications of the ribose-phosphate backbone may be done for a variety of reasons, e.g. to increase the stability and half-life of such molecules in physiological environments or as probes on a biochip. Mixtures of naturally occurring nucleic acids and analogs can be made; alternatively, mixtures of different nucleic acid analogs, and mixtures of naturally occurring nucleic acids and analogs may be made.

[0065] Particularly preferred are peptide nucleic acids (PNA) which includes peptide nucleic acid analogs. These backbones are substantially non-ionic under neutral conditions, in contrast to the highly charged phosphodiester backbone of naturally occurring nucleic acids. This results in two advantages. First, the PNA backbone exhibits improved hybridization kinetics. PNAs have larger changes in the melting temperature (T_(m)) for mismatched versus perfectly matched basepairs. DNA and RNA typically exhibit a 2-4° C. drop in T_(m) for an internal mismatch. With the non-ionic PNA backbone, the drop is closer to 7-9° C. Similarly, due to their non-ionic nature, hybridization of the bases attached to these backbones is relatively insensitive to salt concentration. In addition, PNAs are not degraded by cellular enzymes, and thus can be more stable.

[0066] The nucleic acids may be single stranded or double stranded, as specified, or contain portions of both double stranded or single stranded sequence. As will be appreciated by those in the art, the depiction of a single strand also defines the sequence of the complementary strand; thus the sequences described herein also provide the complement of the sequence. The nucleic acid may be DNA, both genomic and cDNA, RNA or a hybrid, where the nucleic acid may contain combinations of deoxyribo- and ribo-nucleotides, and combinations of bases, including uracil, adenine, thymine, cytosine, guanine, inosine, xanthine hypoxanthine, isocytosine, isoguanine, etc. “Transcript” typically refers to a naturally occurring RNA, e.g., a pre-mRNA, hnRNA, or mRNA. As used herein, the term “nucleoside” includes nucleotides and nucleoside and nucleotide analogs, and modified nucleosides such as amino modified nucleosides. In addition, “nucleoside” includes non-naturally occurring analog structures. Thus, e.g. the individual units of a peptide nucleic acid, each containing a base, are referred to herein as a nucleoside.

[0067] A “label” or a “detectable moiety” is a composition detectable by spectroscopic, photochemical, biochemical, immunochemical, chemical, or other physical means. For example, useful labels include ³²P, fluorescent dyes, electron-dense reagents, enzymes (e.g., as commonly used in an ELISA), biotin, digoxigenin, or haptens and proteins or other entities which can be made detectable, e.g., by incorporating a radiolabel into the peptide or used to detect antibodies specifically reactive with the peptide.

[0068] An “effector” or “effector moiety” or “effector component” is a molecule that is bound (or linked, or conjugated), either covalently, through a linker or a chemical bond, or noncovalently, through ionic, van der Waals, electrostatic, or hydrogen bonds, to an antibody. The “effector” can be a variety of molecules including, e.g., detection moieties including radioactive compounds, fluorescent compounds, an enzyme or substrate, tags such as epitope tags, a toxin; activatable moieties, a chemotherapeutic agent; a lipase; an antibiotic; or a radioisotope emitting “hard” e.g., beta radiation.

[0069] A “labeled nucleic acid probe or oligonucleotide” is one that is bound, either covalently, through a linker or a chemical bond, or noncovalently, through ionic, van der Waals, electrostatic, or hydrogen bonds to a label such that the presence of the probe may be detected by detecting the presence of the label bound to the probe. Alternatively, method using high affinity interactions may achieve the same results where one of a pair of binding partners binds to the other, e.g., biotin, streptavidin.

[0070] As used herein a “nucleic acid probe or oligonucleotide” is defined as a nucleic acid capable of binding to a target nucleic acid of complementary sequence through one or more types of chemical bonds, usually through complementary base pairing, usually through hydrogen bond formation. As used herein, a probe may include natural (i.e., A, G, C, or T) or modified bases (7-deazaguanosine, inosine, etc.). In addition, the bases in a probe may be joined by a linkage other than a phosphodiester bond, so long as it does not functionally interfere with hybridization. Thus, e.g., probes may be peptide nucleic acids in which the constituent bases are joined by peptide bonds rather than phosphodiester linkages. It will be understood by one of skill in the art that probes may bind target sequences lacking complete complementarity with the probe sequence depending upon the stringency of the hybridization conditions. The probes are preferably directly labeled as with isotopes, chromophores, lumiphores, chromogens, or indirectly labeled such as with biotin to which a streptavidin complex may later bind. By assaying for the presence or absence of the probe, one can detect the presence or absence of the select sequence or subsequence. Diagnosis or prognosis may be based at the genomic level, or at the level of RNA or protein expression.

[0071] The term “recombinant” when used with reference, e.g., to a cell, or nucleic acid, protein, or vector, indicates that the cell, nucleic acid, protein or vector, has been modified by the introduction of a heterologous nucleic acid or protein or the alteration of a native nucleic acid or protein, or that the cell is derived from a cell so modified. Thus, e.g., recombinant cells express genes that are not found within the native (non-recombinant) form of the cell or express native genes that are otherwise abnormally expressed, under expressed or not expressed at all. By the term “recombinant nucleic acid” herein is meant nucleic acid, originally formed in vitro, in general, by the manipulation of nucleic acid, e.g., using polymerases and endonucleases, in a form not normally found in nature. In this manner, operably linkage of different sequences is achieved. Thus an isolated nucleic acid, in a linear form, or an expression vector formed in vitro by ligating DNA molecules that are not normally joined, are both considered recombinant for the purposes of this invention. It is understood that once a recombinant nucleic acid is made and reintroduced into a host cell or organism, it will replicate non-recombinantly, i.e., using the in vivo cellular machinery of the host cell rather than in vitro manipulations; however, such nucleic acids, once produced recombinantly, although subsequently replicated non-recombinantly, are still considered recombinant for the purposes of the invention. Similarly, a “recombinant protein” is a protein made using recombinant techniques, i.e., through the expression of a recombinant nucleic acid as depicted above.

[0072] The term “heterologous” when used with reference to portions of a nucleic acid indicates that the nucleic acid comprises two or more subsequences that are not normally found in the same relationship to each other in nature. For instance, the nucleic acid is typically recombinantly produced, having two or more sequences, e.g., from unrelated genes arranged to make a new functional nucleic acid, e.g., a promoter from one source and a coding region from another source. Similarly, a heterologous protein will often refer to two or more subsequences that are not found in the same relationship to each other in nature (e.g., a fusion protein).

[0073] A “promoter” is defined as an array of nucleic acid control sequences that direct transcription of a nucleic acid. As used herein, a promoter includes necessary nucleic acid sequences near the start site of transcription, such as, in the case of a polymerase II type promoter, a TATA element. A promoter also optionally includes distal enhancer or repressor elements, which can be located as much as several thousand base pairs from the start site of transcription. A “constitutive” promoter is a promoter that is active under most environmental and developmental conditions. An “inducible” promoter is a promoter that is active under environmental or developmental regulation. The term “operably linked” refers to a functional linkage between a nucleic acid expression control sequence (such as a promoter, or array of transcription factor binding sites) and a second nucleic acid sequence, wherein the expression control sequence directs transcription of the nucleic acid corresponding to the second sequence.

[0074] An “expression vector” is a nucleic acid construct, generated recombinantly or synthetically, with a series of specified nucleic acid elements that permit transcription of a particular nucleic acid in a host cell. The expression vector can be part of a plasmid, virus, or nucleic acid fragment. Typically, the expression vector includes a nucleic acid to be transcribed operably linked to a promoter.

[0075] The phrase “selectively (or specifically) hybridizes to” refers to the binding, duplexing, or hybridizing of a molecule only to a particular nucleotide sequence under stringent hybridization conditions when that sequence is present in a complex mixture (e.g., total cellular or library DNA or RNA).

[0076] The phrase “stringent hybridization conditions” refers to conditions under which a probe will hybridize to its target subsequence, typically in a complex mixture of nucleic acids, but to essentially no other sequences. Stringent conditions are sequence-dependent and will be different in different circumstances. Longer sequences hybridize specifically at higher temperatures. An extensive guide to the hybridization of nucleic acids is found in Tijssen, Techniques in Biochemistry and Molecular Biology—Hybridization with Nucleic Probes, “Overview of principles of hybridization and the strategy of nucleic acid assays” (1993). Generally, stringent conditions are selected to be about 5-10° C. lower than the thermal melting point (T_(m)) for the specific sequence at a defined ionic strength pH. The T_(m) is the temperature (under defined ionic strength, pH, and nucleic concentration) at which 50% of the probes complementary to the target hybridize to the target sequence at equilibrium (as the target sequences are present in excess, at T_(m), 50% of the probes are occupied at equilibrium). Stringent conditions will be those in which the salt concentration is less than about 1.0 M sodium ion, typically about 0.01 to 1.0 M sodium ion concentration (or other salts) at pH 7.0 to 8.3 and the temperature is at least about 30° C. for short probes (e.g., 10 to 50 nucleotides) and at least about 60° C. for long probes (e.g., greater than 50 nucleotides). Stringent conditions may also be achieved with the addition of destabilizing agents such as formamide. For selective or specific hybridization, a positive signal is at least two times background, preferably 10 times background hybridization. Exemplary stringent hybridization conditions are often: 50% formamide, 5×SSC, and 1% SDS, incubating at 42° C., or, 5×SSC, 1% SDS, incubating at 65° C., with wash in 0.2×SSC, and 0.1% SDS at 65° C. For PCR, a temperature of about 36° C. is typical for low stringency amplification, although annealing temperatures may vary between about 32° C. and 48° C. depending on primer length. For high stringency PCR amplification, a temperature of about 62° C. is typical, although high stringency annealing temperatures can range from about 50° C. to about 65° C., depending on the primer length and specificity. Typical cycle conditions for both high and low stringency amplifications include a denaturation phase of 90° C.-95° C. for 30 sec—2 min., an annealing phase lasting 30 sec.—2 min., and an extension phase of about 72° C. for 1-2 min. Protocols and guidelines for low and high stringency amplification reactions are provided, e.g., in Innis et al., PCR Protocols, A Guide to Methods and Applications (1990).

[0077] Nucleic acids that do not hybridize to each other under stringent conditions are still substantially identical if the polypeptides which they encode are substantially identical. This occurs, e.g., when a copy of a nucleic acid is created using the maximum codon degeneracy permitted by the genetic code. In such cases, the nucleic acids typically hybridize under moderately stringent hybridization conditions. Exemplary “moderately stringent hybridization conditions” include a hybridization in a buffer of 40% formamide, 1 M NaCl, 1% SDS at 37° C., and a wash in 1×SSC at 45° C. A positive hybridization is at least twice background. Those of ordinary skill will readily recognize that alternative hybridization and wash conditions can be utilized to provide conditions of similar stringency. Additional guidelines for determining hybridization parameters are provided in numerous reference, e.g., and Current Protocols in Molecular Biology, ed. Ausubel, et al.

[0078] The phrase “functional effects” in the context of assays for testing compounds that modulate activity of a metastatic colorectal cancer protein includes the determination of a parameter that is indirectly or directly under the influence of the metastatic colorectal cancer protein or nucleic acid, e.g., an enzymatic, functional, physical, or chemical effect, such as the ability to decrease metastatic colorectal cancer. It includes ligand binding activity; cell growth on soft agar; anchorage dependence; contact inhibition and density limitation of growth; cellular proliferation; cellular transformation; growth factor or serum dependence; tumor specific marker levels; invasiveness into Matrigel; tumor growth and metastasis in vivo; mRNA and protein expression in cells undergoing metastasis, and other characteristics of metastatic colorectal cancer cells. “Functional effects” include in vitro, in vivo, and ex vivo activities.

[0079] By “determining the functional effect” is meant assaying for a compound that increases or decreases a parameter that is indirectly or directly under the influence of a metastatic colorectal cancer protein sequence, e.g., functional, enzymatic, physical and chemical effects. Such functional effects can be measured by any means known to those skilled in the art, e.g., changes in spectroscopic characteristics (e.g., fluorescence, absorbance, refractive index), hydrodynamic (e.g., shape), chromatographic, or solubility properties for the protein, measuring inducible markers or transcriptional activation of the metastatic colorectal cancer protein; measuring binding activity or binding assays, e.g., binding to antibodies or other ligands, and measuring cellular proliferation. Determination of the functional effect of a compound on metastatic colorectal cancer can also be performed using metastatic colorectal cancer assays known to those of skill in the art such as an in vitro assays, e.g., cell growth on soft agar; anchorage dependence; contact inhibition and density limitation of growth; cellular proliferation; cellular transformation; growth factor or serum dependence; tumor specific marker levels; invasiveness into Matrigel; tumor growth and metastasis in vivo; mRNA and protein expression in cells undergoing metastasis, and other characteristics of metastatic colorectal cancer cells. The functional effects can be evaluated by many means known to those skilled in the art, e.g., microscopy for quantitative or qualitative measures of alterations in morphological features, measurement of changes in RNA or protein levels for metastatic colorectal cancer-associated sequences, measurement of RNA stability, identification of downstream or reporter gene expression (CAT, luciferase, β-gal, GFP and the like), e.g., via chemiluminescence, fluorescence, colorimetric reactions, antibody binding, inducible markers, and ligand binding assays.

[0080] “Ihiibitors”, “activators”, and “modulators” of metastatic colorectal cancer polynucleotide and polypeptide sequences are used to refer to activating, inhibitory, or modulating molecules or compounds identified using in vitro and in vivo assays of metastatic colorectal cancer polynucleotide and polypeptide sequences of the invention. Inhibitors are compounds that, e.g., bind to, partially or totally block activity, decrease, prevent, delay activation, inactivate, desensitize, or down regulate the activity or expression of metastatic colorectal cancer proteins of the invention, e.g., antagonists. Antisense nucleic acids may seem to inhibit expression and subsequent function of the protein. “Activators” are compounds that increase, open, activate, facilitate, enhance activation, sensitize, agonize, or up regulate metastatic colorectal cancer protein activity. Inhibitors, activators, or modulators also include genetically modified versions of metastatic colorectal cancer proteins, e.g., versions with altered activity, as well as naturally occurring and synthetic ligands, antagonists, agonists, antibodies, small chemical molecules and the like. Such assays for inhibitors and activators include, e.g., expressing the metastatic colorectal cancer protein in vitro, in cells, or cell membranes, applying putative modulator compounds, and then determining the functional effects on activity, as described above. Activators and inhibitors of metastatic colorectal cancer can also be identified by incubating metastatic colorectal cancer cells with the test compound and determining increases or decreases in the expression of 1 or more metastatic colorectal cancer proteins, e.g., 1, 2, 3, 4, 5, 10, 15, 20, 25, 30, 40, 50 or more metastatic colorectal cancer proteins, such as colorectal cancer proteins encoded by the sequences set out in Tables 1-26.

[0081] Samples or assays comprising metastatic colorectal cancer proteins that are treated with a potential activator, inhibitor, or modulator are compared to control samples without the inhibitor, activator, or modulator to examine the extent of inhibition. Control samples (untreated with inhibitors) are assigned a relative protein activity value of 100%. Inhibition of a polypeptide is achieved when the activity value relative to the control is about 80%, preferably 50%, more preferably 25-0%. Activation of a metastatic colorectal cancer polypeptide is achieved when the activity value relative to the control (untreated with activators) is 110%, more preferably 150%, more preferably 200-500% (i.e., two to five fold higher relative to the control), more preferably 1000-3000% higher.

[0082] The phrase “changes in cell growth” refers to any change in cell growth and proliferation characteristics in vitro or in vivo, such as formation of foci, anchorage independence, semi-solid or soft agar growth, changes in contact inhibition and density limitation of growth, loss of growth factor or serum requirements, changes in cell morphology, gaining or losing immortalization, gaining or losing tumor specific markers, ability to form or suppress tumors when injected into suitable animal hosts, and/or immortalization of the cell. See, e.g., Freshney, Culture of Animal Cells a Manual of Basic Technique pp. 231-241 (3^(rd) ed. 1994).

[0083] “Tumor cell” refers to precancerous, cancerous, and normal cells in a tumor.

[0084] “Cancer cells,” “transformed” cells or “transformation” in tissue culture, refers to spontaneous or induced phenotypic changes that do not necessarily involve the uptake of new genetic material. Although transformation can arise from infection with a transforming virus and incorporation of new genomic DNA, or uptake of exogenous DNA, it can also arise spontaneously or following exposure to a carcinogen, thereby mutating an endogenous gene. Transformation is associated with phenotypic changes, such as immortalization of cells, aberrant growth control, nonmorphological changes, and/or malignancy (see, Freshney, Culture of Animal Cells a Manual of Basic Technique (3^(rd) ed. 1994)).

[0085] “Antibody” refers to a polypeptide comprising a framework region from an immunoglobulin gene or fragments thereof that specifically binds and recognizes an antigen. The recognized immunoglobulin genes include the kappa, lambda, alpha, gamma, delta, epsilon, and mu constant region genes, as well as the myriad immunoglobulin variable region genes. Light chains are classified as either kappa or lambda. Heavy chains are classified as gamma, mu, alpha, delta, or epsilon, which in turn define the immunoglobulin classes, IgG, IgM, IgA, IgD and IgE, respectively. Typically, the antigen-binding region of an antibody or its functional equivalent will be most critical in specificity and affinity of binding. See Paul, Fundamental Immunology.

[0086] An exemplary immunoglobulin (antibody) structural unit comprises a tetramer. Each tetramer is composed of two identical pairs of polypeptide chains, each pair having one “light” (about 25 kD) and one “heavy” chain (about 50-70 kD). The N-terminus of each chain defines a variable region of about 100 to 110 or more amino acids primarily responsible for antigen recognition. The terms variable light chain (V_(L)) and variable heavy chain (V_(H)) refer to these light and heavy chains respectively.

[0087] Antibodies exist, e.g., as intact immunoglobulins or as a number of well-characterized fragments produced by digestion with various peptidases. Thus, e.g., pepsin digests an antibody below the disulfide linkages in the hinge region to produce F(ab′)₂, a dimer of Fab which itself is a light chain joined to V_(H)-C_(H)1 by a disulfide bond. The F(ab′)₂ may be reduced under mild conditions to break the disulfide linkage in the hinge region, thereby converting the F(ab′)′₂ dimer into an Fab′ monomer. The Fab′ monomer is essentially Fab with part of the hinge region (see Fundamental Immunology (Paul ed., 3d ed. 1993). While various antibody fragments are defined in terms of the digestion of an intact antibody, one of skill will appreciate that such fragments may be synthesized de novo either chemically or by using recombinant DNA methodology. Thus, the term antibody, as used herein, also includes antibody fragments either produced by the modification of whole antibodies, or those synthesized de novo using recombinant DNA methodologies (e.g., single chain Fv) or those identified using phage display libraries (see, e.g., McCafferty et al., Nature 348:552-554 (1990))

[0088] For preparation of antibodies, e.g., recombinant, monoclonal, or polyclonal antibodies, many technique known in the art can be used (see, e.g. Kohler & Milstein, Nature 256:495-497 (1975); Kozbor et al., Immunology Today 4:72 (1983); Cole et al., pp. 77-96 in Monoclonal Antibodies and Cancer Therapy (1985); Coligan, Current Protocols in Immunology (1991); Harlow & Lane, Antibodies, A Laboratory Manual (1988); and Goding, Monoclonal Antibodies: Principles and Practice (2d ed. 1986)). Techniques for the production of single chain antibodies (U.S. Pat. No. 4,946,778) can be adapted to produce antibodies to polypeptides of this invention. Also, transgenic mice, or other organisms such as other mammals, may be used to express humanized antibodies. Alternatively, phage display technology can be used to identify antibodies and heteromeric Fab fragments that specifically bind to selected antigens (see, e.g., McCafferty et al., Nature 348:552-554 (1990); Marks et al., Biotechnology 10:779-783 (1992)).

[0089] A “chimeric antibody” is an antibody molecule in which, e.g, (a) the constant region, or a portion thereof, is altered, replaced or exchanged so that the antigen binding site (variable region) is linked to a constant region of a different or altered class, effector function and/or species, or an entirely different molecule which confers new properties to the chimeric antibody, e.g., an enzyme, toxin, hormone, growth factor, drug, etc.; or (b) the variable region, or a portion thereof, is altered, replaced or exchanged with a variable region having a different or altered antigen specificity.

[0090] Identification of Metastatic Colorectal Cancer-Associated Sequences

[0091] In one aspect, the expression levels of genes are determined in different patient samples for which diagnosis information is desired, to provide expression profiles. An expression profile of a particular sample is essentially a “fingerprint” of the state of the .sample; while two states may have any particular gene similarly expressed, the evaluation of a number of genes simultaneously allows the generation of a gene expression profile that is characteristic of the state of the cell. That is, normal tissue may be distinguished from cancerous or metastatic cancerous tissue, or metastatic cancerous tissue can be compared with tissue from surviving cancer patients. By comparing expression profiles of tissue in known different metastatic colorectal cancer states, information regarding which genes are important (including both up- and down-regulation of genes) in each of these states is obtained.

[0092] The identification of sequences that are differentially expressed in metastatic colorectal cancer versus non-metastatic colorectal cancer tissue allows the use of this information in a number of ways. For example, a particular treatment regime may be evaluated: does a chemotherapeutic drug act to down-regulate metastatic colorectal cancer, and thus tumor growth or recurrence, in a particular patient. Similarly, diagnosis and treatment outcomes may be done or confirmed by comparing patient samples with the known expression profiles. Metastatic tissue can also be analyzed to determine the stage of metastatic colorectal cancer in the tissue. Furthermore, these gene expression profiles (or individual genes) allow screening of drug candidates with an eye to mimicking or altering a particular expression profile; e.g., screening can be done for drugs that suppress the metastatic colorectal cancer expression profile. This may be done by making biochips comprising sets of the important metastatic colorectal cancer genes, which can then be used in these screens. PCR methods may be applied with selected primer pairs, and analysis may be of RNA or of genomic sequences. These methods can also be done on the protein basis; that is, protein expression levels of the metastatic colorectal cancer proteins can be evaluated for diagnostic purposes or to screen candidate agents. In addition, the metastatic colorectal cancer nucleic acid sequences can be administered for gene therapy purposes, including the administration of antisense nucleic acids, or the metastatic colorectal cancer proteins (including antibodies and other modulators thereof) administered as therapeutic drugs or as protein or DNA vaccines.

[0093] Thus the present invention provides nucleic acid and protein sequences that are differentially expressed in metastatic colorectal cancer, herein termed “metastatic colorectal cancer sequences.” As outlined below, metastatic colorectal cancer sequences include those that are up-regulated (i.e., expressed at a higher level) in metastatic colorectal cancer, as well as those that are down-regulated (i.e., expressed at a lower level). In a preferred embodiment, the metastatic colorectal cancer sequences are from humans; however, as will be appreciated by those in the art, metastatic colorectal cancer sequences from other organisms may be useful in animal models of disease and drug evaluation; thus, other metastatic colorectal cancer sequences are provided, from vertebrates, including mammals, including rodents (rats, mice, hamsters, guinea pigs, etc.), primates, farm animals (including sheep, goats, pigs, cows, horses, etc.) and pets (dogs, cats, etc.). Metastatic colorectal cancer sequences from other organisms may be obtained using the techniques outlined below.

[0094] Metastatic colorectal cancer sequences can include both nucleic acid and amino acid sequences. As will be appreciated by those in the art and is more fully outlined below, metastatic colorectal cancer nucleic acid sequences are useful in a variety of applications, including diagnostic applications, which will detect naturally occurring nucleic acids, as well as screening applications; e.g., biochips comprising nucleic acid probes or PCR microtiter plates with selected probes to the metastatic colorectal cancer sequences can be generated.

[0095] A metastatic colorectal cancer sequence can be initially identified by substantial nucleic acid and/or amino acid sequence homology to the metastatic colorectal cancer sequences outlined herein. Such homology can be based upon the overall nucleic acid or amino acid sequence, and is generally determined as outlined below, using either homology programs or hybridization conditions.

[0096] For identifying metastatic colorectal cancer-associated sequences, the metastatic colorectal cancer screen typically includes comparing genes identified in different tissues, e.g., normal and cancerous tissues, or tumor tissue samples from patients who have metastatic disease vs. non metastatic tissue, or tumor tissue samples from patients who have been diagnosed with Dukes stage A or B cancer but have survived vs. metastatic tissue. Other suitable tissue comparisons include comparing metastatic colorectal cancer samples with metastatic cancer samples from other cancers, such as lung, breast, other gastrointestinal cancers, prostate, ovarian, etc. Samples of, e.g., Dukes stage B survivor tissue and tissue undergoing metastasis are applied to biochips comprising nucleic acid probes. The samples are first microdissected, if applicable, and treated as is known in the art for the preparation of mRNA. Suitable biochips are commercially available, e.g., from Affymetrix. Gene expression profiles as described herein are generated and the data analyzed.

[0097] In one embodiment, the genes showing changes in expression as between normal and disease states are compared to genes expressed in other normal tissues, preferably normal colon, but also including, and not limited to lung, heart, brain, liver, breast, kidney, muscle, prostate, small intestine, large intestine, spleen, bone and placenta. In a preferred embodiment, those genes identified during the metastatic colorectal cancer screen that are expressed in significant amounts in other tissues are removed from the profile, although in some embodiments, this is not necessary. That is, when screening for drugs, it is usually preferable that the target be disease specific, to minimize possible side effects.

[0098] In a preferred embodiment, metastatic colorectal cancer sequences are those that are up-regulated in metastatic colorectal cancer; that is, the expression of these genes is higher in the metastatic tissue as compared to non-metastatic cancerous tissue or normal colon tissue (see, e.g., Tables 1-26). “Up-regulation” as used herein means, when the ratio is presented as a number greater than one, that the ratio is greater than one, preferably 1.5 or greater, more preferably 2.0 or greater. All UniGene cluster identification numbers and accession numbers herein are for the GenBank sequence database and the sequences of the accession numbers are hereby expressly incorporated by reference. GenBank is known in the art, see, e.g., Benson, DA, et al., Nucleic Acids Research 26:1-7 (1998) and http://www.ncbi.nlm.nih.gov/. Sequences are also available in other databases, e.g., European Molecular Biology Laboratory (EMBL) and DNA Database of Japan (DDBJ).

[0099] In another preferred embodiment, metastatic colorectal cancer sequences are those that are down-regulated in the metastatic colorectal cancer; that is, the expression of these genes is lower in metastatic tissue as compared to non-metastatic cancerous tissue or normal colon tissue (see, e.g., Tables 1-26). “Down-regulation” as used herein means, when the ratio is presented as a number greater than one, that the ratio is greater than one, preferably 1.5 or greater, more preferably 2.0 or greater, or, when the ratio is presented as a number less than one, that the ratio is less than one, preferably 0.5 or less, more preferably 0.25 or less.

[0100] Informatics

[0101] The ability to identify genes that are over or under expressed in metastatic colorectal cancer can additionally provide high-resolution, high-sensitivity datasets which can be used in the areas of diagnostics, therapeutics, drug development, pharmacogenetics, protein structure, biosensor development, and other related areas. For example, the expression profiles can be used in diagnostic or prognostic evaluation of patients with metastatic colorectal cancer. Or as another example, subcellular toxicological information can be generated to better direct drug structure and activity correlation (see Anderson, Pharmaceutical Proteomics: Targets, Mechanism, and Function, paper presented at the IBC Proteomics conference, Coronado, Calif. (Jun. 11-12, 1998)). Subcellular toxicological information can also be utilized in a biological sensor device to predict the likely toxicological effect of chemical exposures and likely tolerable exposure thresholds (see U.S. Pat. No. 5,811,231). Similar advantages accrue from datasets relevant to other biomolecules and bioactive agents (e.g., nucleic acids, saccharides, lipids, drugs, and the like).

[0102] Thus, in another embodiment, the present invention provides a database that includes at least one set of assay data. The data contained in the database is acquired, e.g., using array analysis either singly or in a library format. The database can be in substantially any form in which data can be maintained and transmitted, but is preferably an electronic database. The electronic database of the invention can be maintained on any electronic device allowing for the storage of and access to the database, such as a personal computer, but is preferably distributed on a wide area network, such as the World Wide Web.

[0103] The focus of the present section on databases that include peptide sequence data is for clarity of illustration only. It will be apparent to those of skill in the art that similar databases can be assembled for assay data acquired using an assay of the invention.

[0104] The compositions and methods for identifying and/or quantitating the relative and/or absolute abundance of a variety of molecular and macromolecular species from a biological sample undergoing metastatic colorectal cancer, i.e., the identification of metastatic colorectal cancer-associated sequences described herein, provide an abundance of information, which can be correlated with pathological conditions, predisposition to disease, drug testing, therapeutic monitoring, gene-disease causal linkages, identification of correlates of immunity and physiological status, among others. Although the data generated from the assays of the invention is suited for manual review and analysis, in a preferred embodiment, prior data processing using high-speed computers is utilized.

[0105] An array of methods for indexing and retrieving biomolecular information is known in the art. For example, U.S. Pat. Nos. 6,023,659 and 5,966,712 disclose a relational database system for storing biomolecular sequence information in a manner that allows sequences to be catalogued and searched according to one or more protein function hierarchies. U.S. Pat. No. 5,953,727 discloses a relational database having sequence records containing information in a format that allows a collection of partial-length DNA sequences to be catalogued and searched according to association with one or more sequencing projects for obtaining full-length sequences from the collection of partial length sequences. U.S. Pat. No. 5,706,498 discloses a gene database retrieval system for making a retrieval of a gene sequence similar to a sequence data item in a gene database based on the degree of similarity between a key sequence and a target sequence. U.S. Pat. No. 5,538,897 discloses a method using mass spectroscopy fragmentation patterns of peptides to identify amino acid sequences in computer databases by comparison of predicted mass spectra with experimentally-derived mass spectra using a closeness-of-fit measure. U.S. Pat. No. 5,926,818 discloses a multi-dimensional database comprising a functionality for multi-dimensional data analysis described as on-line analytical processing (OLAP), which entails the consolidation of projected and actual data according to more than one consolidation path or dimension. U.S. Pat. No. 5,295,261 reports a hybrid database structure in which the fields of each database record are divided into two classes, navigational and informational data, with navigational fields stored in a hierarchical topological map which can be viewed as a tree structure or as the merger of two or more such tree structures.

[0106] See also Mount et al., Bioinformatics (2001); Biological Sequence Analysis: Probabilistic Models of Proteins and Nucleic Acids (Durbin et al., eds., 1999); Bioinformatics: A Practical Guide to the Analysis of Genes and Proteins (Baxevanis & Oeullette eds., 1998)); Rashidi & Buehler, Bioinformatics: Basic Applications in Biological Science and Medicine (1999); Introduction to Computational Molecular Biology (Setubal et al., eds 1997); Bioinformatics: Methods and Protocols (Misener & Krawetz, eds, 2000); Bioinformatics: Sequence, Structure, and Databanks: A Practical Approach (Higgins & Taylor, eds., 2000); Brown, Bioinformatics: A Biologist's Guide to Biocomputing and the Internet (2001); Han & Kamber, Data Mining: Concepts and Techniques (2000); and Waterman, Introduction to Computational Biology: Maps, Sequences, and Genomes (1995).

[0107] The present invention provides a computer database comprising a computer and software for storing in computer-retrievable form assay data records cross-tabulated, e.g., with data specifying the source of the target-containing sample from which each sequence specificity record was obtained.

[0108] In an exemplary embodiment, at least one of the sources of target-containing sample is from a control tissue sample known to be free of pathological disorders. In a variation, at least one of the sources is a known pathological tissue specimen, e.g., a neoplastic lesion or another tissue specimen to be analyzed for metastatic colorectal cancer. In another variation, the assay records cross-tabulate one or more of the following parameters for each target species in a sample: (1) a unique identification code, which can include, e.g., a target molecular structure and/or characteristic separation coordinate (e.g., electrophoretic coordinates); (2) sample source; and (3) absolute and/or relative quantity of the target species present in the sample.

[0109] The invention also provides for the storage and retrieval of a collection of target data in a computer data storage apparatus, which can include magnetic disks, optical disks, magneto-optical disks, DRAM, SRAM, SGRAM, SDRAM, RDRAM, DDR RAM, magnetic bubble memory devices, and other data storage devices, including CPU registers and on-CPU data storage arrays. Typically, the target data records are stored as a bit pattern in an array of magnetic domains on a magnetizable medium or as an array of charge states or transistor gate states, such as an array of cells in a DRAM device (e.g., each cell comprised of a transistor and a charge storage area, which may be on the transistor). In one embodiment, the invention provides such storage devices, and computer systems built therewith, comprising a bit pattern encoding a protein expression fingerprint record comprising unique identifiers for at least 10 target data records cross-tabulated with target source.

[0110] When the target is a peptide or nucleic acid, the invention preferably provides a method for identifying related peptide or nucleic acid sequences, comprising performing a computerized comparison between a peptide or nucleic acid sequence assay record stored in or retrieved from a computer storage device or database and at least one other sequence. The comparison can include a sequence analysis or comparison algorithm or computer program embodiment thereof (e.g., FASTA, TFASTA, GAP, BESTFIT) and/or the comparison may be of the relative amount of a peptide or nucleic acid sequence in a pool of sequences determined from a polypeptide or nucleic acid sample of a specimen.

[0111] The invention also preferably provides a magnetic disk, such as an IBM-compatible (DOS, Windows, Windows95/98/2000, Windows NT, OS/2) or other format (e.g., Linux, SunOS, Solaris, AIX, SCO Unix, VMS, MV, Macintosh, etc.) floppy diskette or hard (fixed, Winchester) disk drive, comprising a bit pattern encoding data from an assay of the invention in a file format suitable for retrieval and processing in a computerized sequence analysis, comparison, or relative quantitation method.

[0112] The invention also provides a network, comprising a plurality of computing devices linked via a data link, such as an Ethernet cable (coax or 10BaseT), telephone line, ISDN line, wireless network, optical fiber, or other suitable signal transmission medium, whereby at least one network device (e.g., computer, disk array, etc.) comprises a pattern of magnetic domains (e.g., magnetic disk) and/or charge domains (e.g., an array of DRAM cells) composing a bit pattern encoding data acquired from an assay of the invention.

[0113] The invention also provides a method for transmitting assay data that includes generating an electronic signal on an electronic communications device, such as a modem, ISDN terminal adapter, DSL, cable modem, ATM switch, or the like, wherein the signal includes (in native or encrypted format) a bit pattern encoding data from an assay or a database comprising a plurality of assay results obtained by the method of the invention.

[0114] In a preferred embodiment, the invention provides a computer system for comparing a query target to a database containing an array of data structures, such as an assay result obtained by the method of the invention, and ranking database targets based on the degree of identity and gap weight to the target data. A central processor is preferably initialized to load and execute the computer program for alignment and/or comparison of the assay results. Data for a query target is entered into the central processor via an I/O device. Execution of the computer program results in the central processor retrieving the assay data from the data file, which comprises a binary description of an assay result.

[0115] The target data or record and the computer program can be transferred to secondary memory, which is typically random access memory (e.g., DRAM, SRAM, SGRAM, or SDRAM). Targets are ranked according to the degree of correspondence between a selected assay characteristic (e.g., binding to a selected affinity moiety) and the same characteristic of the query target and results are output via an I/O device. For example, a central processor can be a conventional computer (e.g., Intel Pentium, PowerPC, Alpha, PA-8000, SPARC, MIPS 4400, MIPS 10000, VAX, etc.); a program can be a commercial or public domain molecular biology software package (e.g., UWGCG Sequence Analysis Software, Darwin); a data file can be an optical or magnetic disk, a data server, a memory device (e.g., DRAM, SRAM, SGRAM, SDRAM, EPROM, bubble memory, flash memory, etc.); an I/O device can be a terminal comprising a video display and a keyboard, a modem, an ISDN terminal adapter, an Ethernet port, a punched card reader, a magnetic strip reader, or other suitable I/O device.

[0116] The invention also preferably provides the use of a computer system, such as that described above, which comprises: (1) a computer; (2) a stored bit pattern encoding a collection of peptide sequence specificity records obtained by the methods of the invention, which may be stored in the computer; (3) a comparison target, such as a query target; and (4) a program for alignment and comparison, typically with rank-ordering of comparison results on the basis of computed similarity values.

[0117] Characteristics of Metastatic Colorectal Cancer-Associated Proteins

[0118] Metastatic colorectal cancer proteins of the present invention may be classified as secreted proteins, transmembrane proteins or intracellular proteins. In one embodiment, the metastatic colorectal cancer protein is an intracellular protein. Intracellular proteins may be found in the cytoplasm and/or in the nucleus and/or in the organelles. Proteins containing one or more transmembrane domains that exclusively reside in organelles are also considered intracellular proteins. Intracellular proteins are involved in all aspects of cellular function and replication (including, e.g., signaling pathways); aberrant expression of such proteins often results in unregulated or disregulated cellular processes (see, e.g., Molecular Biology of the Cell (Alberts, ed., 3rd ed., 1994). For example, many intracellular proteins have enzymatic activity such as protein kinase activity, protein phosphatase activity, protease activity, nucleotide cyclase activity, polymerase activity and the like. Intracellular proteins also serve as docking proteins that are involved in organizing complexes of proteins, or targeting proteins to various subcellular localizations, and are involved in maintaining the structural integrity of organelles.

[0119] An increasingly appreciated concept in characterizing proteins is the presence in the proteins of one or more motifs for which defined functions have been attributed. In addition to the highly conserved sequences found in the enzymatic domain of proteins, highly conserved sequences have been identified in proteins that are involved in protein-protein interaction. For example, Src-homology-2 (SH2) domains bind tyrosine-phosphorylated targets in a sequence dependent manner. PTB domains, which are distinct from SH2 domains, also bind tyrosine phosphorylated targets. SH3 domains bind to proline-rich targets. In addition, PH domains, tetratricopeptide repeats and WD domains to name only a few, have been shown to mediate protein-protein interactions. Some of these may also be involved in binding to phospholipids or other second messengers. As will be appreciated by one of ordinary skill in the art, these motifs can be identified on the basis of primary sequence; thus, an analysis of the sequence of proteins may provide insight into both the enzymatic potential of the molecule and/or molecules with which the protein may associate. One useful database is Pfam (protein families), which is a large collection of multiple sequence alignments and hidden Markov models covering many common protein domains. Versions are available via the internet from Washington University in St. Louis, the Sanger Center in England, and the Karolinska Institute in Sweden (see, e.g., Bateman et al., Nuc. Acids Res. 28:263-266 (2000); Sonnhammer et al., Proteins 28:405-420 (1997); Bateman et al., Nuc. Acids Res. 27:260-262 (1999); and Sonnharnmer et al., Nuc. Acids Res. 26:320-322-(1998)).

[0120] In another embodiment, the metastatic colorectal cancer sequences are transmembrane proteins. Transmembrane proteins are molecules that span a phospholipid bilayer of a cell. They may have an intracellular domain, an extracellular domain, or both. The intracellular domains of such proteins may have a number of functions including those already described for intracellular proteins. For example, the intracellular domain may have enzymatic activity and/or may serve as a binding site for additional proteins. Frequently the intracellular domain of transmembrane proteins serves both roles. For example certain receptor tyrosine kinases have both protein kinase activity and SH2 domains. In addition, autophosphorylation of tyrosines on the receptor molecule itself, creates binding sites for additional SH2 domain containing proteins.

[0121] Transmembrane proteins may contain from one to many transmembrane domains. For example, receptor tyrosine kinases, certain cytokine receptors, receptor guanylyl cyclases and receptor serine/threonine protein kinases contain a single transmembrane domain. However, various other proteins including channels, pumps, and adenylyl cyclases contain numerous transmembrane domains. Many important cell surface receptors such as G protein coupled receptors (GPCRs) are classified as “seven transmembrane domain” proteins, as they contain 7 membrane spanning regions. Characteristics of transmembrane domains include approximately 20 consecutive hydrophobic amino acids that may be followed by charged amino acids. Therefore, upon analysis of the amino acid sequence of a particular protein, the localization and number of transmembrane domains within the protein may be predicted (see, e.g. PSORT web site http://psort.nibb.ac.jp/).

[0122] The extracellular domains of transmembrane proteins are diverse; however, conserved motifs are found repeatedly among various extracellular domains. Conserved structure and/or functions have been ascribed to different extracellular motifs. Many extracellular domains are involved in binding to other molecules. In one aspect, extracellular domains are found on receptors. Factors that bind the receptor domain include circulating ligands, which may be peptides, proteins, or small molecules such as adenosine and the like. For example, growth factors such as EGF, FGF and PDGF are circulating growth factors that bind to their cognate receptors to initiate a variety of cellular responses. Other factors include cytokines, mitogenic factors, hormones, neurotrophic factors and the like. Extracellular domains also bind to cell-associated molecules. In this respect, they mediate cell-cell interactions. Cell-associated ligands can be tethered to the cell, e.g., via a glycosylphosphatidylinositol (GPI) anchor, or may themselves be transmembrane proteins. Extracellular domains also associate with the extracellular matrix and contribute to the maintenance of the cell structure.

[0123] Metastatic colorectal cancer proteins that are transmembrane are particularly preferred in the present invention as they are readily accessible targets for extracellular immunotherapeutics, as are described herein. In addition, as outlined below, transmembrane proteins can be also useful in imaging modalities. Antibodies may be used to label such readily accessible proteins in situ or in histological analysis. Alternatively, antibodies can also label intracellular proteins, in which case analytical samples are typically permeablized to provide access to intracellular proteins.

[0124] It will also be appreciated by those in the art that a transmembrane protein can be made soluble by removing transmembrane sequences, e.g., through recombinant methods. Furthermore, transmembrane proteins that have been made soluble can be made to be secreted through recombinant means by adding an appropriate signal sequence.

[0125] In another embodiment, the metastatic colorectal cancer proteins are secreted proteins; the secretion of which can be either constitutive or regulated. These proteins have a signal peptide or signal sequence that targets the molecule to the secretory pathway. Secreted proteins are involved in numerous physiological events; by virtue of their circulating nature, they often serve to transmit signals to various other cell types. The secreted protein may function in an autocrine manner (acting on the cell that secreted the factor), a paracrine manner (acting on cells in close proximity to the cell that secreted the factor) or an endocrine manner (acting on cells at a distance). Thus secreted molecules find use in modulating or altering numerous aspects of physiology. Metastatic colorectal cancer proteins that are secreted proteins are particularly preferred in the present invention as they serve as good targets for diagnostic markers, e.g., for blood, plasma, serum, or stool tests.

[0126] Use of Metastatic Colorectal Cancer Nucleic Acids

[0127] As described above, metastatic colorectal cancer sequence is initially identified by substantial nucleic acid and/or amino acid sequence homology or linkage to the metastatic colorectal cancer sequences outlined herein. Such homology can be based upon the overall nucleic acid or amino acid sequence, and is generally determined as outlined below, using either homology programs or hybridization conditions. Typically, linked sequences on a mRNA are found on the same molecule. The metastatic colorectal cancer nucleic acid sequences of the invention, e.g., the sequences in Tables 1-26, can be fragments of larger genes, i.e., they are nucleic acid segments. “Genes” in this context includes coding regions, non-coding regions, and mixtures of coding and non-coding regions. Accordingly, as will be appreciated by those in the art, using the sequences provided herein, extended sequences, in either direction, of the metastatic colorectal cancer genes can be obtained, using techniques well known in the art for cloning either longer sequences or the full length sequences; see Ausubel, et al., supra. Much can be done by informatics and many sequences can be clustered to include multiple sequences corresponding to a single gene, e.g., systems such as UniGene (see, http://www.ncbi.nlm.nih.gov/unigene/).

[0128] Once the metastatic colorectal cancer nucleic acid is identified, it can be cloned and, if necessary, its constituent parts recombined to form the entire metastatic colorectal cancer nucleic acid coding regions or the entire mRNA sequence. Once isolated from its natural source, e.g., contained within a plasmid or other vector or excised therefrom as a linear nucleic acid segment, the recombinant metastatic colorectal cancer nucleic acid can be further-used as a probe to identify and isolate other metastatic colorectal cancer nucleic acids, e.g., extended coding regions. It can also be used as a “precursor” nucleic acid to make modified or variant metastatic colorectal cancer nucleic acids and proteins.

[0129] The metastatic colorectal cancer nucleic acids of the present invention are used in several ways. In a first embodiment, nucleic acid probes to the metastatic colorectal cancer nucleic acids are made and attached to biochips to be used in screening and diagnostic methods, as outlined below, or for administration, e.g., for gene therapy, vaccine, and/or antisense applications. Alternatively, the metastatic colorectal cancer nucleic acids that include coding regions of metastatic colorectal cancer proteins can be put into expression vectors for the expression of metastatic colorectal cancer proteins, again for screening purposes or for administration to a patient.

[0130] In a preferred embodiment, nucleic acid probes to metastatic colorectal cancer nucleic acids (both the nucleic acid sequences outlined in the figures and/or the complements thereof) are made. The nucleic acid probes attached to the biochip are designed to be substantially complementary to the metastatic colorectal cancer nucleic acids, i.e. the target sequence (either the target sequence of the sample or to other probe sequences, e.g., in sandwich assays), such that hybridization of the target sequence and the probes of the present invention occurs. As outlined below, this complementarity need not be perfect; there may be any number of base pair mismatches which will interfere with hybridization between the target sequence and the single stranded nucleic acids of the present invention. However, if the number of mutations is so great that no hybridization can occur under even the least stringent of hybridization conditions, the sequence is not a complementary target sequence. Thus, by “substantially complementary” herein is meant that the probes are sufficiently complementary to the target sequences to hybridize under appropriate reaction conditions, particularly high stringency conditions, as outlined herein.

[0131] A nucleic acid probe is generally single stranded but can be partially single and partially double stranded. The strandedness of the probe is dictated by the structure, composition, and properties of the target sequence. In general, the nucleic acid probes range from about 8 to about 100 bases long, with from about 10 to about 80 bases being preferred, and from about 30 to about 50 bases being particularly preferred. That is, generally complements of ORFs or whole genes are not used. In some embodiments, nucleic acids of lengths up to hundreds of bases can be used.

[0132] In a preferred embodiment, more than one probe per sequence is used, with either overlapping probes or probes to different sections of the target being used. That is, two, three, four or more probes, with three being preferred, are used to build in a redundancy for a particular target. The probes can be overlapping (i.e., have some sequence in common), or separate. In some cases, PCR primers may be used to amplify signal for higher sensitivity.

[0133] As will be appreciated by those in the art, nucleic acids can be attached or immobilized to a solid support in a wide variety of ways. By “immobilized” and grammatical equivalents herein is meant the association or binding between the nucleic acid probe and the solid support is sufficient to be stable under the conditions of binding, washing, analysis, and removal as outlined below. The binding can typically be covalent or non-covalent. By “non-covalent binding” and grammatical equivalents herein is typically meant one or more of electrostatic, hydrophilic, and hydrophobic interactions. Included in non-covalent binding is the covalent attachment of a molecule, such as, streptavidin to the support and the non-covalent binding of the biotinylated probe to the streptavidin. By “covalent binding” and grammatical equivalents herein is meant that the two moieties, the solid support and the probe, are attached by at least one bond, including sigma bonds, pi bonds and coordination bonds. Covalent bonds can be formed directly between the probe and the solid support or can be formed by a cross linker or by inclusion of a specific reactive group on either the solid support or the probe or both molecules. Immobilization may also involve a combination of covalent and non-covalent interactions.

[0134] In general, the probes are attached to a biochip in a wide variety of ways, as will be appreciated by those in the art. As described herein, the nucleic acids can either be synthesized first, with subsequent attachment to the biochip, or can be directly synthesized on the biochip.

[0135] The biochip comprises a suitable solid substrate. By “substrate” or “solid support” or other grammatical equivalents herein is meant a material that can be modified to contain discrete individual sites appropriate for the attachment or association of the nucleic acid probes and is amenable to at least one detection method. As will be appreciated by those in the art, the number of possible substrates are very large, and include, but are not limited to, glass and modified or functionalized glass, plastics (including acrylics, polystyrene and copolymers of styrene and other materials, polypropylene, polyethylene, polybutylene, polyurethanes, Teflon, etc.), polysaccharides, nylon or nitrocellulose, resins, silica or silica-based materials including silicon and modified silicon, carbon, metals, inorganic glasses, plastics, etc. In general, the substrates allow optical detection and do not appreciably fluoresce. A preferred substrate is described in copending application entitled Reusable Low Fluorescent Plastic Biochip, U.S. application Ser. No. 09/270,214, filed Mar. 15, 1999, herein incorporated by reference in its entirety.

[0136] Generally the substrate is planar, although as will be appreciated by those in the art, other configurations of substrates may be used as well. For example, the probes may be placed on the inside surface of a tube, for flow-through sample analysis to minimize sample volume. Similarly, the substrate may be flexible, such as a flexible foam, including closed cell foams made of particular plastics.

[0137] In a preferred embodiment, the surface of the biochip and the probe may be derivatized with chemical functional groups for subsequent attachment of the two. Thus, e.g., the biochip is derivatized with a chemical functional group including, but not limited to, amino groups, carboxy groups, oxo groups and thiol groups, with amino groups being particularly preferred. Using these functional groups, the probes can be attached using functional groups on the probes. For example, nucleic acids containing amino groups can be attached to surfaces comprising amino groups, e.g., using linkers as are known in the art; e.g., homo-or hetero-bifunctional linkers as are well known (see 1994 Pierce Chemical Company catalog, technical section on cross-linkers, pages 155-200). In addition, in some cases, additional linkers, such as alkyl groups (including substituted and heteroalkyl groups) may be used.

[0138] In this embodiment, oligonucleotides are synthesized as is known in the art, and then attached to the surface of the solid support. As will be appreciated by those skilled in the art, either the 5′ or 3′ terminus may be attached to the solid support, or attachment may be via an internal nucleoside.

[0139] In another embodiment, the immobilization to the solid support may be very strong, yet non-covalent. For example, biotinylated oligonucleotides can be made, which bind to surfaces covalently coated with streptavidin, resulting in attachment.

[0140] Alternatively, the oligonucleotides may be synthesized on the surface, as is known in the art. For example, photoactivation techniques utilizing photopolymerization compounds and techniques are used. In a preferred embodiment, the nucleic acids can be synthesized in situ, using well known photolithographic techniques, such as those described in WO 95/25116; WO 95/35505; U.S. Pat. Nos. 5,700,637 and 5,445,934; and references cited within, all of which are expressly incorporated by reference; these methods of attachment form the basis of the Affimetrix GeneChip™ technology.

[0141] Often, amplification-based assays are performed to measure the expression level of metastatic colorectal cancer-associated sequences. These assays are typically performed in conjunction with reverse transcription. In such assays, a metastatic colorectal cancer-associated nucleic acid sequence acts as a template in an amplification reaction (e.g., Polymerase Chain Reaction, or PCR). In a quantitative amplification, the amount of amplification product will be proportional to the amount of template in the original sample. Comparison to appropriate controls provides a measure of the amount of metastatic colorectal cancer-associated RNA. Methods of quantitative amplification are well known to those of skill in the art. Detailed protocols for quantitative PCR are provided, e.g., in Innis et al., PCR Protocols, A Guide to Methods and Applications (1990).

[0142] In some embodiments, a TaqMan based assay is used to measure expression. TaqMan based assays use a fluorogenic oligonucleotide probe that contains a 5′ fluorescent dye and a 3′ quenching agent. The probe hybridizes to a PCR product, but cannot itself be extended due to a blocking agent at the 3′ end. When the PCR product is amplified in subsequent cycles, the 5′ nuclease activity of the polymerase, e.g., AmpliTaq, results in the cleavage of the TaqMan probe. This cleavage separates the 5′ fluorescent dye and the 3′ quenching agent, thereby resulting in an increase in fluorescence as a function of amplification (see, e.g., literature provided by Perkin-Elmer, e.g., www2.perkin-elmer.com).

[0143] Other suitable amplification methods include, but are not limited to, ligase chain reaction (LCR) (see Wu & Wallace, Genomics 4:560 (1989), Landegren et al., Science 241:1077 (1988), and Barringer et al., Gene 89:117 (1990)), transcription amplification (Kwoh et al., Proc. Natl. Acad. Sci. USA 86:1173 (1989)), self-sustained sequence replication (Guatelli et al., Proc. Nat. Acad. Sci. USA 87:1874 (1990)), dot PCR, and linker adapter PCR, etc.

[0144] Expression of Metastatic Colorectal Cancer Proteins From Nucleic Acids

[0145] In a preferred embodiment, metastatic colorectal cancer nucleic acids, e.g., encoding metastatic colorectal cancer proteins, are used to make a variety of expression vectors to express metastatic colorectal cancer proteins which can then be used in screening assays, as described below. Expression vectors and recombinant DNA technology are well known to those of skill in the art (see, e.g., Ausubel, supra, and Gene Expression Systems (Fernandez & Hoeffler, eds, 1999)) and are used to express proteins. The expression vectors may be either self-replicating extrachromosomal vectors or vectors which integrate into a host genome. Generally, these expression vectors include transcriptional and translational regulatory nucleic acid operably linked to the nucleic acid encoding the metastatic colorectal cancer protein. The term “control sequences” refers to DNA sequences used for the expression of an operably linked coding sequence in a particular host organism. Control sequences that are suitable for prokaryotes, e.g., include a promoter, optionally an operator sequence, and a ribosome binding site. Eukaryotic cells are known to utilize promoters, polyadenylation signals, and enhancers.

[0146] Nucleic acid is “operably linked” when it is placed into a functional relationship with another nucleic acid sequence. For example, DNA for a presequence or secretory leader is operably linked to DNA for a polypeptide if it is expressed as a preprotein that participates in the secretion of the polypeptide; a promoter or enhancer is operably linked to a coding sequence if it affects the transcription of the sequence; or a ribosome binding site is operably linked to a coding sequence if it is positioned so as to facilitate translation. Generally, “operably linked” means that the DNA sequences being linked are contiguous, and, in the case of a secretory leader, contiguous and in reading phase. However, enhancers do not have to be contiguous. Linking is typically accomplished by ligation at convenient restriction sites. If such sites do not exist, synthetic oligonucleotide adaptors or linkers are used in accordance with conventional practice. Transcriptional and translational regulatory nucleic acid will generally be appropriate to the host cell used to express the metastatic colorectal cancer protein. Numerous types of appropriate expression vectors, and suitable regulatory sequences are known in the art for a variety of host cells.

[0147] In general, transcriptional and translational regulatory sequences may include, but are not limited to, promoter sequences, ribosomal binding sites, transcriptional start and stop sequences, translational start and stop sequences, and enhancer or activator sequences. In a preferred embodiment, the regulatory sequences include a promoter and transcriptional start and stop sequences.

[0148] Promoter sequences encode either constitutive or inducible promoters. The promoters may be either naturally occurring promoters or hybrid promoters. Hybrid promoters, which combine elements of more than one promoter, are also known in the art, and are useful in the present invention.

[0149] In addition, an expression vector may comprise additional elements. For example, the expression vector may have two replication systems, thus allowing it to be maintained in two organisms, e.g., in mammalian or insect cells for expression and in a procaryotic host for cloning and amplification. Furthermore, for integrating expression vectors, the expression vector contains at least one sequence homologous to the host cell genome, and preferably two homologous sequences which flank the expression construct. The integrating vector may be directed to a specific locus in the host cell by selecting the appropriate homologous sequence for inclusion in the vector. Constructs for integrating vectors are well known in the art (e.g., Fernandez & Hoeffler, supra).

[0150] In addition, in a preferred embodiment, the expression vector contains a selectable marker gene to allow the selection of transformed host cells. Selection genes are well known in the art and will vary with the host cell used.

[0151] The metastatic colorectal cancer proteins of the present invention are produced by culturing a host cell transformed with an expression vector containing nucleic acid encoding a metastatic colorectal cancer protein, under the appropriate conditions to induce or cause expression of the metastatic colorectal cancer protein. Conditions appropriate for metastatic colorectal cancer protein expression will vary with the choice of the expression vector and the host cell, and will be easily ascertained by one skilled in the art through routine experimentation or optimization. For example, the use of constitutive promoters in the expression vector will require optimizing the growth and proliferation of the host cell, while the use of an inducible promoter requires the appropriate growth conditions for induction. In addition, in some embodiments, the timing of the harvest is important. For example, the baculoviral systems used in insect cell expression are lytic viruses, and thus harvest time selection can be crucial for product yield.

[0152] Appropriate host cells include yeast, bacteria, archaebacteria, fungi, and insect and animal cells, including mammalian cells. Of particular interest are Saccharomyces cerevisiae and other yeasts, E. coli, Bacillus subtilis, Sf9 cells, C129 cells, 293 cells, Neurospora, BHK, CHO, COS, HeLa cells, HLVEC (human umbilical vein endothelial cells), THP1 cells (a macrophage cell line) and various other human cells and cell lines.

[0153] In a preferred embodiment, the metastatic colorectal cancer proteins are expressed in mammalian cells. Mammalian expression systems are also known in the art, and include retroviral and adenoviral systems. Of particular use as mammalian promoters are the promoters from mammalian viral genes, since the viral genes are often highly expressed and have a broad host range. Examples include the SV40 early promoter, mouse mammary tumor virus LTR promoter, adenovirus major late promoter, herpes simplex virus promoter, and the CMV promoter (see, e.g., Fernandez & Hoeffler, supra). Typically, transcription termination and polyadenylation sequences recognized by mammalian cells are regulatory regions located 3′ to the translation stop codon and thus, together with the promoter elements, flank the coding sequence. Examples of transcription terminator and polyadenylation signals include those derived form SV40.

[0154] The methods of introducing exogenous nucleic acid into mammalian hosts, as well as other hosts, is well known in the art, and will vary with the host cell used. Techniques include dextran-mediated transfection, calcium phosphate precipitation, polybrene mediated transfection, protoplast fusion, electroporation, viral infection, encapsulation of the polynucleotide(s) in liposomes, and direct microinjection of the DNA into nuclei.

[0155] In a preferred embodiment, metastatic colorectal cancer proteins are expressed in bacterial systems. Promoters from bacteriophage may also be used and are known in the art. In addition, synthetic promoters and hybrid promoters are also useful; e.g., the tac promoter is a hybrid of the trp and lac promoter sequences. Furthermore, a bacterial promoter can include naturally occurring promoters of non-bacterial origin that have the ability to bind bacterial RNA polymerase and initiate transcription. In addition to a functioning promoter sequence, an efficient ribosome binding site is desirable. The expression vector may also include a signal peptide sequence that provides for secretion of the metastatic colorectal cancer protein in bacteria. The protein is either secreted into the growth media (gram-positive bacteria) or into the periplasmic space, located between the inner and outer membrane of the cell (gram-negative bacteria). The bacterial expression vector may also include a selectable marker gene to allow for the selection of bacterial strains that have been transformed. Suitable selection genes include genes which render the bacteria resistant to drugs such as ampicillin, chloramphenicol, erythromycin, kanamycin, neomycin and tetracycline. Selectable markers also include biosynthetic genes, such as those in the histidine, tryptophan and leucine biosynthetic pathways. These components are assembled into expression vectors. Expression vectors for bacteria are well known in the art, and include vectors for Bacillus subtilis, E. coli, Streptococcus cremoris, and Streptococcus lividans, among others (e.g., Fernandez & Hoeffler, supra). The bacterial expression vectors are transformed into bacterial host cells using techniques well known in the art, such as calcium chloride treatment, electroporation, and others.

[0156] In one embodiment, metastatic colorectal cancer proteins are produced in insect cells. Expression vectors for the transformation of insect cells, and in particular, baculovirus-based expression vectors, are well known in the art.

[0157] In a preferred embodiment, metastatic colorectal cancer protein is produced in yeast cells. Yeast expression systems are well known in the art, and include expression vectors for Saccharomyces cerevisiae, Candida albicans and C. maltosa, Hansenula polymorpha, Kluyveromyces fragilis and K. lactis, Pichia guillerimondii and P. pastoris, Schizosaccharomyces pombe, and Yarrowia lipolytica.

[0158] The metastatic colorectal cancer protein may also be made as a fusion protein, using techniques well known in the art. Thus, e.g., for the creation of monoclonal antibodies, if the desired epitope is small, the metastatic colorectal cancer protein may be fused to a carrier protein to form an immunogen. Alternatively, the metastatic colorectal cancer protein may be made as a fusion protein to increase expression for affinity purification purposes, or for other reasons. For example, when the metastatic colorectal cancer protein is a metastatic colorectal cancer peptide, the nucleic acid encoding the peptide may be linked to other nucleic acid for expression purposes.

[0159] In a preferred embodiment, the metastatic colorectal cancer protein is purified or isolated after expression. Metastatic colorectal cancer proteins may be isolated or purified in a variety of appropriate ways. Standard purification methods include electrophoretic, molecular, immunological and chromatographic techniques, including ion exchange, hydrophobic, affinity, and reverse-phase HPLC chromatography, and chromatofocusing. For example, the metastatic colorectal cancer protein may be purified using a standard anti-metastatic colorectal cancer protein antibody column. Ultrafiltration and diafiltration techniques, in conjunction with protein concentration, are also useful. For general guidance in suitable purification techniques, see Scopes, Protein Purification (1982). The degree of purification necessary will vary depending on the use of the metastatic colorectal cancer protein. In some instances no purification will be necessary.

[0160] Once expressed and purified if necessary, the metastatic colorectal cancer proteins and nucleic acids are useful in a number of applications. They may be used as immunoselection reagents, as vaccine reagents, as screening agents, etc.

[0161] Variants of Metastatic Colorectal Cancer Proteins

[0162] In one embodiment, the metastatic colorectal cancer proteins are derivative or variant metastatic colorectal cancer proteins as compared to the wild-type sequence. That is, as outlined more fully below, the derivative metastatic colorectal cancer peptide will often contain at least one amino acid substitution, deletion or insertion, with amino acid substitutions being particularly preferred. The amino acid substitution, insertion or deletion may occur at a particular residue within the metastatic colorectal cancer peptide.

[0163] Also included within one embodiment of metastatic colorectal cancer proteins of the present invention are amino acid sequence variants. These variants typically fall into one or more of three classes: substitutional, insertional or deletional variants. These variants ordinarily are prepared by site specific mutagenesis of nucleotides in the DNA encoding the metastatic colorectal cancer protein, using cassette or PCR mutagenesis or other techniques, to produce DNA encoding the variant, and thereafter expressing the DNA in recombinant cell culture as outlined above. However, variant metastatic colorectal cancer protein fragments having up to about 100-150 residues may be prepared by in vitro synthesis. Amino acid sequence variants are characterized by the predetermined nature of the variation, a feature that sets them apart from naturally occurring allelic or interspecies variation of the metastatic colorectal cancer protein amino acid sequence. The variants typically exhibit the same qualitative biological activity as the naturally occurring analogue, although variants can also be selected which have modified characteristics as will be more fully outlined below.

[0164] While the site or region for introducing an amino acid sequence variation is often predetermined, the mutation per se need not be predetermined. For example, in order to optimize the performance of a mutation at a given site, random mutagenesis may be conducted at the target codon or region and the expressed metastatic colorectal cancer variants screened for the optimal combination of desired activity. Techniques exist for making substitution mutations at predetermined sites in DNA having a known sequence, e.g., M13 primer mutagenesis and PCR mutagenesis. Screening of the mutants is done using assays of metastatic colorectal cancer protein activities.

[0165] Amino acid substitutions are typically of single residues; insertions usually will be on the order of from about 1 to 20 amino acids, although considerably larger insertions may be occasionally tolerated. Deletions range from about 1 to about 20 residues, although in some cases deletions may be much larger.

[0166] Substitutions, deletions, insertions or any combination thereof may be used to arrive at a final derivative. Generally these changes are done on a few amino acids to minimize the alteration of the molecule. Larger changes may be tolerated in certain circumstances. When small alterations in the characteristics of a metastatic colorectal cancer protein are desired, substitutions are generally made in accordance with the amino acid substitution chart provided in the definition section.

[0167] Variants typically exhibit the same qualitative biological activity and will elicit the same immune response as the naturally-occurring analog, although variants also are selected to modify the characteristics of the metastatic colorectal cancer proteins as needed. Alternatively, the variant may be designed or reorganized such that the biological activity of the metastatic colorectal cancer protein is altered. For example, glycosylation sites may be altered or removed.

[0168] Covalent modifications of metastatic colorectal cancer polypeptides are included within the scope of this invention. One type of covalent modification includes reacting targeted amino acid residues of a metastatic colorectal cancer polypeptide with an organic derivatizing agent that is capable of reacting with selected side chains or the N-or C-terminal residues of a metastatic colorectal cancer polypeptide. Derivatization with bifunctional agents is useful, for instance, for crosslinking metastatic colorectal cancer polypeptides to a water-insoluble support matrix or surface for use in the method for purifying anti-metastatic colorectal cancer polypeptide antibodies or screening assays, as is more fully described below. Commonly used crosslinking agents include, e.g., 1,1-bis(diazoacetyl)-2-phenylethane, glutaraldehyde, N-hydroxysuccinimide esters, e.g., esters with 4-azidosalicylic acid, homobifunctional imidoesters, including disuccinimidyl esters such as 3,3′-dithiobis(succinimidylpropionate), bifunctional maleimides such as bis-N-maleimido-1,8-octane and agents such as methyl-3-((p-azidophenyl)dithio)propioimidate.

[0169] Other modifications include deamidation of glutaminyl and asparaginyl residues to the corresponding glutamyl and aspartyl residues, respectively, hydroxylation of proline and lysine, phosphorylation of hydroxyl groups of seryl, threonyl or tyrosyl residues, methylation of the γ-amino groups of lysine, arginine, and histidine side chains (Creighton, Proteins: Structure and Molecular Properties, pp. 79-86 (1983)), acetylation of the N-terminal amine, and amidation of any C-terminal carboxyl group.

[0170] Another type of covalent modification of the metastatic colorectal cancer polypeptide encompassed by this invention is an altered native glycosylation pattern of the polypeptide. “Altering the native glycosylation pattern” is intended herein to mean adding to or deleting one or more carbohydrate moieties of a native sequence metastatic colorectal cancer polypeptide. Glycosylation patterns can be altered in many ways. For example the use of different cell types to express metastatic colorectal cancer-associated sequences can result in different glycosylation patterns.

[0171] Addition of glycosylation sites to metastatic colorectal cancer polypeptides may also be accomplished by altering the amino acid sequence thereof. The alteration may be made, e.g., by the addition of, or substitution by, one or more serine or threonine residues to the native sequence metastatic colorectal cancer polypeptide (for O-linked glycosylation sites). The metastatic colorectal cancer amino acid sequence may optionally be altered through changes at the DNA level, particularly by mutating the DNA encoding the metastatic colorectal cancer polypeptide at preselected bases such that codons are generated that will translate into the desired amino acids.

[0172] Another means of increasing the number of carbohydrate moieties on the metastatic colorectal cancer polypeptide is by chemical or enzymatic coupling of glycosides to the polypeptide. Such methods are described in the art, e.g., in WO 87/05330, and in Aplin & Wriston, CRC Crit. Rev. Biochem., pp. 259-306 (1981).

[0173] Removal of carbohydrate moieties present on the metastatic colorectal cancer polypeptide may be accomplished chemically or enzymatically or by mutational substitution of codons encoding for amino acid residues that serve as targets for glycosylation. Chemical deglycosylation techniques are known in the art and described, for instance, by Hakimuddin, et al., Arch. Biochem. Biophys., 259:52 (1987) and by Edge et al., Anal. Biochem., 118:131 (1981). Enzymatic cleavage of carbohydrate moieties on polypeptides can be achieved by the use of a variety of endo-and exo-glycosidases as described by Thotakura et al., Meth. Enzymol., 138:350 (1987).

[0174] Another type of covalent modification of metastatic colorectal cancer comprises linking the metastatic colorectal cancer polypeptide to one of a variety of nonproteinaceous polymers, e.g., polyethylene glycol, polypropylene glycol, or polyoxyalkylenes, in the manner set forth in U.S. Pat. Nos. 4,640,835; 4,496,689; 4,301,144; 4,670,417; 4,791,192 or 4,179,337.

[0175] Metastatic colorectal cancer polypeptides of the present invention may also be modified in a way to form chimeric molecules comprising a metastatic colorectal cancer polypeptide fused to another, heterologous polypeptide or amino acid sequence. In one embodiment, such a chimeric molecule comprises a fusion of a metastatic colorectal cancer polypeptide with a tag polypeptide which provides an epitope to which an anti-tag antibody can selectively bind. The epitope tag is generally placed at the amino-or carboxyl-terminus of the metastatic colorectal cancer polypeptide. The presence of such epitope-tagged forms of a metastatic colorectal cancer polypeptide can be detected using an antibody against the tag polypeptide. Also, provision of the epitope tag enables the metastatic colorectal cancer polypeptide to be readily purified by affinity purification using an anti-tag antibody or another type of affinity matrix that binds to the epitope tag. In an alternative embodiment, the chimeric molecule may comprise a fusion of a metastatic colorectal cancer polypeptide with an immunoglobulin or a particular region of an immunoglobulin. For a bivalent form of the chimeric molecule, such a fusion could be to the Fc region of an IgG molecule.

[0176] Various tag polypeptides and their respective antibodies are well known and examples include poly-histidine (poly-his) or poly-histidine-glycine (poly-his-gly) tags; HIS6 and metal chelation tags, the flu HA tag polypeptide and its antibody 12CA5 (Field et al., Mol. Cell. Biol. 8:2159-2165 (1988)); the c-myc tag and the 8F9, 3C7, 6E10, G4, B7 and 9E10 antibodies thereto (Evan et al., Molecular and Cellular Biology 5:3610-3616 (1985)); and the Herpes Simplex virus glycoprotein D (gD) tag and its antibody (Paborsky et al., Protein Engineering 3(6):547-553 (1990)). Other tag polypeptides include the Flag-peptide (Hopp et al., BioTechnology 6:1204-1210 (1988)); the KT3 epitope peptide (Martin et al., Science 255:192-194 (1992)); tubulin epitope peptide (Skinner et al., J. Biol. Chem. 266:15163-15166 (1991)); and the T7 gene 10 protein peptide tag (Lutz-Freyermuth et al., Proc. Natl. Acad. Sci. USA 87:6393-6397 (1990)).

[0177] Also included are other metastatic colorectal cancer proteins of the metastatic colorectal cancer family, and metastatic colorectal cancer proteins from other organisms, which are cloned and expressed as outlined below. Thus, probe or degenerate polymerase chain reaction (PCR) primer sequences may be used to find other related metastatic colorectal cancer proteins from primates or other organisms. As will be appreciated by those in the art, particularly useful probe and/or PCR primer sequences include unique areas of the metastatic colorectal cancer nucleic acid sequence. As is generally known in the art, preferred PCR primers are from about 15 to about 35 nucleotides in length, with from about 20 to about 30 being preferred, and may contain inosine as needed. PCR reaction conditions are well known in the art (e.g., Innis, PCR Protocols, supra).

[0178] Antibodies to Metastatic colorectal Cancer Proteins

[0179] In a preferred embodiment, when a metastatic colorectal cancer protein is to be used to generate antibodies, e.g., for immunotherapy or immunodiagnosis, the metastatic colorectal cancer protein should share at least one epitope or determinant with the full length protein. By “epitope” or “determinant” herein is typically meant a portion of a protein which will generate and/or bind an antibody or T-cell receptor in the context of MHC. Thus, in most instances, antibodies made to a smaller metastatic colorectal cancer protein will be able to bind to the full-length protein, particularly linear epitopes. In a preferred embodiment, the epitope is unique; that is, antibodies generated to a unique epitope show little or no cross-reactivity.

[0180] Methods of preparing polyclonal antibodies are well known (e.g., Coligan, supra; and Harlow & Lane, supra). Polyclonal antibodies can be raised in a mammal, e.g., by one or more injections of an immunizing agent and, if desired, an adjuvant. Typically, the immunizing agent and/or adjuvant will be injected in the mammal by multiple subcutaneous or intraperitoneal injections. The immunizing agent may include a protein encoded by a nucleic acid of Tables 1-26 or fragment thereof or a fusion protein thereof. It may be useful to conjugate the immunizing agent to a protein known to be immunogenic in the mammal being immunized. Immunogenic proteins include, e.g., keyhole limpet hemocyanin, serum albumin, bovine thyroglobulin, and soybean trypsin inhibitor. Adjuvants include, e.g., Freund's complete adjuvant and MPL-TDM adjuvant (monophosphoryl Lipid A, synthetic trehalose dicorynomycolate). The immunization protocol may be selected by one skilled in the art.

[0181] The antibodies may, alternatively, be monoclonal antibodies. Monoclonal antibodies may be prepared using hybridoma methods, such as those described by Kohler & Milstein, Nature 256:495 (1975). In a hybridoma method, a mouse, hamster, or other appropriate host animal, is typically immunized with an immunizing agent to elicit lymphocytes that produce or are capable of producing antibodies that will specifically bind to the immunizing agent. Alternatively, the lymphocytes may be immunized in vitro. The immunizing agent will typically include a polypeptide encoded by a nucleic acid of Tables 1-26, or fragment thereof, or a fusion protein thereof Generally, either peripheral blood lymphocytes (“PBLs”) are used if cells of human origin are desired, or spleen cells or lymph node cells are used if non-human mammalian sources are desired. The lymphocytes are then fused with an immortalized cell line using a suitable fusing agent, such as polyethylene glycol, to form a hybridoma cell (Goding, Monoclonal Antibodies: Principles and Practice, pp. 59-103 (1986)). Immortalized cell lines are usually transformed mammalian cells, particularly myeloma cells of rodent, bovine and primate origin. Usually, rat or mouse myeloma cell lines are employed. The hybridoma cells may be cultured in a suitable culture medium that preferably contains one or more substances that inhibit the growth or survival of the unfused, immortalized cells. For example, if the parental cells lack the enzyme hypoxanthine guanine phosphoribosyl transferase (HGPRT or HPRT), the culture medium for the hybridomas typically will include hypoxanthine, aminopterin, and thymidine (“HAT medium”), which substances prevent the growth of HGPRT-deficient cells.

[0182] In one embodiment, the antibodies are bispecific antibodies. Bispecific antibodies are typically monoclonal, preferably human or humanized, antibodies that have binding specificities for at least two different antigens or that have binding specificities for two epitopes on the same antigen. In one embodiment, one of the binding specificities is for a protein encoded by a nucleic acid of Tables 1-26 or a fragment thereof, the other one is for any other antigen, and preferably for a cell-surface protein or receptor or receptor subunit, preferably one that is tumor specific. Alternatively, tetramer-type technology may create multivalent reagents.

[0183] In a preferred embodiment, the antibodies to metastatic colorectal cancer protein are capable of reducing or eliminating a biological function of a metastatic colorectal cancer protein, as is described below. That is, the addition of anti-metastatic colorectal cancer protein antibodies (either polyclonal or preferably monoclonal) to metastatic colorectal cancer tissue (or cells containing metastatic colorectal cancer) may reduce or eliminate the metastatic colorectal cancer. Generally, at least a 25% decrease in activity, growth, size or the like is preferred, with at least about 50% being particularly preferred and about a 95-100% decrease being especially preferred.

[0184] In a preferred embodiment the antibodies to the metastatic colorectal cancer proteins are humanized antibodies (e.g., Xenerex Biosciences, Mederex, Inc., Abgenix, Inc., Protein Design Labs, Inc.) Humanized forms of non-human (e.g., murine) antibodies are chimeric molecules of immunoglobulins, immunoglobulin chains or fragments thereof (such as Fv, Fab, Fab′, F(ab′)2 or other antigen-binding subsequences of antibodies) which contain minimal sequence derived from non-human immunoglobulin. Humanized antibodies include human immunoglobulins (recipient antibody) in which residues from a complementary determining region (CDR) of the recipient are replaced by residues from a CDR of a non-human species (donor antibody) such as mouse, rat or rabbit having the desired specificity, affinity and capacity. In some instances, Fv framework residues of the human immunoglobulin are replaced by corresponding non-human residues. Humanized antibodies may also comprise residues which are found neither in the recipient antibody nor in the imported CDR or framework sequences. In general, a humanized antibody will comprise substantially all of at least one, and typically two, variable domains, in which all or substantially all of the CDR regions correspond to those of a non-human immunoglobulin and all or substantially all of the framework (FR) regions are those of a human immunoglobulin consensus sequence. The humanized antibody optimally also will comprise at least a portion of an immunoglobulin constant region (Fc), typically that of a human immunoglobulin (Jones et al., Nature 321:522-525 (1986); Riechmann et al., Nature 332:323-329 (1988); and Presta, Curr. Op. Struct. Biol. 2:593-596 (1992)). Humanization can be essentially performed following the method of Winter and co-workers (Jones et al., Nature 321:522-525 (1986); Riechmann et al., Nature 332:323-327 (1988); Verhoeyen et al., Science 239:1534-1536 (1988)), by substituting rodent CDRs or CDR sequences for the corresponding sequences of a human antibody. Accordingly, such humanized antibodies are chimeric antibodies (U.S. Pat. No. 4,816,567), wherein substantially less than an intact human variable domain has been substituted by the corresponding sequence from a non-human species.

[0185] Human-like antibodies can also be produced using various techniques known in the art, including phage display libraries (Hoogenboom & Winter, J. Mol. Biol. 227:381 (1991); Marks et al., J. Mol. Biol. 222:581 (1991)). The techniques of Cole et al. and Boerner et al. are also available for the preparation of human monoclonal antibodies (Cole et al., Monoclonal Antibodies and Cancer Therapy, p. 77 (1985) and Boerner et al., J. Immunol. 147(1):86-95 (1991)). Similarly, human antibodies can be made by introducing of human immunoglobulin loci into transgenic animals, e.g., mice in which the endogenous immunoglobulin genes have been partially or completely inactivated. Upon challenge, human antibody production is observed, which closely resembles that seen in humans in virtually all respects, including gene rearrangement, assembly, and antibody repertoire. This approach is described, e.g., in U.S. Pat. Nos. 5,545,807; 5,545,806; 5,569,825; 5,625,126; 5,633,425; 5,661,016, and in the following scientific publications: Marks et al., Bio/Technology 10:779-783 (1992); Lonberg et al., Nature 368:856-859 (1994); Morrison, Nature 368:812-13 (1994); Fishwild et al., Nature Biotechnology 14:845-51 (1996); Neuberger, Nature Biotechnology 14:826 (1996); Lonberg & Huszar, Intern. Rev. Immunol. 13:65-93 (1995).

[0186] By immunotherapy is meant treatment of metastatic colorectal cancer with an antibody raised against a metastatic colorectal cancer proteins. As used herein, immunotherapy can be passive or active. Passive immunotherapy as defined herein is the passive transfer of antibody to a recipient (patient). Active immunization is the induction of antibody and/or T-cell responses in a recipient (patient). Induction of an immune response is the result of providing the recipient with an antigen to which antibodies are raised. The antigen may be provided by injecting a polypeptide against which antibodies are desired to be raised into a recipient, or contacting the recipient with a nucleic acid capable of expressing the antigen and under conditions for expression of the antigen, leading to an immune response.

[0187] In a preferred embodiment the metastatic colorectal cancer proteins against which antibodies are raised are secreted proteins as described above. Without being bound by theory, antibodies used for treatment, bind and prevent the secreted protein from binding to its receptor, thereby inactivating the secreted metastatic colorectal cancer protein.

[0188] In another preferred embodiment, the metastatic colorectal cancer protein to which antibodies are raised is a transmembrane protein. Without being bound by theory, antibodies used for this treatment typically bind the extracellular domain of the metastatic colorectal cancer protein and prevent it from binding to other proteins, such as circulating ligands or cell-associated molecules. The antibody may cause down-regulation of the transmembrane metastatic colorectal cancer protein. The antibody may be a competitive, non-competitive or uncompetitive inhibitor of protein binding to the extracellular domain of the metastatic colorectal cancer protein. The antibody may be an antagonist of the metastatic colorectal cancer protein or may prevent activation of the transmembrane metastatic colorectal cancer protein. In some embodiments, when the antibody prevents the binding of other molecules to the metastatic colorectal cancer protein, the antibody prevents growth of the cell. The antibody may also be used to target or sensitize the cell to cytotoxic agents, including, but not limited to TNF-α, TNF-β, IL-1, INF-γ and IL-2, or chemotherapeutic agents including 5FU, vinblastine, actinomycin D, cisplatin, methotrexate, and the like. In some instances the antibody belongs to a sub-type that activates serum complement when complexed with the transmembrane protein thereby mediating cytotoxicity or antigen-dependent cytotoxicity (ADCC). Thus, metastatic colorectal cancer is treated by administering to a patient antibodies directed against the transmembrane metastatic colorectal cancer protein. Antibody-labeling may activate a co-toxin, localize a toxin payload, or otherwise provide means to locally ablate cells.

[0189] In another preferred embodiment, the antibody is conjugated to an effector moiety. The effector moiety can be any number of molecules, including labeling moieties such as radioactive labels or fluorescent labels, or can be a therapeutic moiety. In one aspect the therapeutic moiety is a small molecule that modulates the activity of the metastatic colorectal cancer protein. In another aspect the therapeutic moiety modulates the activity of molecules associated with or in close proximity to the metastatic colorectal cancer protein. The therapeutic moiety may inhibit enzymatic activity such as protease or collagenase activity associated with metastatic colorectal cancer.

[0190] In a preferred embodiment, the therapeutic moiety can also be a cytotoxic agent. In this method, targeting the cytotoxic agent to metastatic colorectal cancer tissue or cells results in a reduction in the number of afflicted cells, thereby reducing symptoms associated with metastatic colorectal cancer. Cytotoxic agents are numerous and varied and include, but are not limited to, cytotoxic drugs or toxins or active fragments of such toxins. Suitable toxins and their corresponding fragments include diphtheria A chain, exotoxin A chain, ricin A chain, abrin A chain, curcin, crotin, phenomycin, enomycin and the like. Cytotoxic agents also include radiochemicals made by conjugating radioisotopes to antibodies raised against metastatic colorectal cancer proteins, or binding of a radionuclide to a chelating agent that has been covalently attached to the antibody. Targeting the therapeutic moiety to transmembrane metastatic colorectal cancer proteins not only serves to increase the local concentration of therapeutic moiety in the metastatic colorectal cancer afflicted area, but also serves to reduce deleterious side effects that may be associated with the therapeutic moiety.

[0191] In another preferred embodiment, the metastatic colorectal cancer protein against which the antibodies are raised is an intracellular protein. In this case, the antibody may be conjugated to a protein or other entity which facilitates entry into the cell. In one case, the antibody enters the cell by endocytosis. In another embodiment, a nucleic acid encoding the antibody is administered to the individual or cell. Moreover, wherein the metastatic colorectal cancer protein can be targeted within a cell, i.e., the nucleus, an antibody thereto contains a signal for that target localization, i.e., a nuclear localization signal.

[0192] The metastatic colorectal cancer antibodies of the invention specifically bind to metastatic colorectal cancer proteins. By “specifically bind” herein is meant that the antibodies bind to the protein with a K_(d) of at least about 0.1 mM, more usually at least about 1 μM, preferably at least about 0.1 μM or better, and most preferably, 0.01 μM or better. Selectivity of binding is also important.

[0193] Detection of Metastatic Colorectal Cancer Sequence for Diagnostic and Therapeutic Applications

[0194] In one aspect, the RNA expression levels of genes are determined for different cellular states in the metastatic colorectal cancer phenotype. Expression levels of genes in normal tissue (i.e., not undergoing metastatic colorectal cancer) and in metastatic colorectal cancer tissue (and in some cases, for varying severities of metastatic colorectal cancer that relate to prognosis, as outlined below) are evaluated to provide expression profiles. An expression profile of a particular cell state or point of development is essentially a “fingerprint” of the state. While two states may have any particular gene similarly expressed, the evaluation of a number of genes simultaneously allows the generation of a gene expression profile that is reflective of the state of the cell. By comparing expression profiles of cells in different states, information regarding which genes are important (including both up- and down-regulation of genes) in each of these states is obtained. Then, diagnosis may be performed or confirmed to determine whether a tissue sample has the gene expression profile of normal or cancerous tissue. This will provide for molecular diagnosis of related conditions.

[0195] “Differential expression,” or grammatical equivalents as used herein, refers to qualitative or quantitative differences in the temporal and/or cellular gene expression patterns within and among cells and tissue. Thus, a differentially expressed gene can qualitatively have its expression altered, including an activation or inactivation, in, e.g., normal versus metastatic colorectal cancer tissue. Genes may be turned on or turned off in a particular state, relative to another state thus permitting comparison of two or more states. A qualitatively regulated gene will exhibit an expression pattern within a state or cell type which is detectable by standard techniques. Some genes will be expressed in one state or cell type, but not in both. Alternatively, the difference in expression may be quantitative, e.g., in that expression is increased or decreased; i.e., gene expression is either upregulated, resulting in an increased amount of transcript, or downregulated, resulting in a decreased amount of transcript. The degree to which expression differs need only be large enough to quantify via standard characterization techniques as outlined below, such as by use of Affymetrix GeneChip™ expression arrays, Lockhart, Nature Biotechnology 14:1675-1680 (1996), hereby expressly incorporated by reference. Other techniques include, but are not limited to, quantitative reverse transcriptase PCR, northern analysis and RNase protection. As outlined above, preferably the change in expression (i.e., upregulation or downregulation) is typically at least about 50%, more preferably at least about 100%, more preferably at least about 150%, more preferably at least about 200%, with from 300 to at least 1000% being especially preferred.

[0196] Evaluation may be at the gene transcript, or the protein level. The amount of gene expression may be monitored using nucleic acid probes to the DNA or RNA equivalent of the gene transcript, and the quantification of gene expression levels, or, alternatively, the final gene product itself (protein) can be monitored, e.g., with antibodies to the metastatic colorectal cancer protein and standard immunoassays (ELISAs, etc.) or other techniques, including mass spectroscopy assays, 2D gel electrophoresis assays, etc. Proteins corresponding to metastatic colorectal cancer genes, i.e., those identified as being important in a metastatic colorectal cancer phenotype, can be evaluated in a metastatic colorectal cancer diagnostic test.

[0197] In a preferred embodiment, gene expression monitoring is performed simultaneously on a number of genes.

[0198] The metastatic colorectal cancer nucleic acid probes may be attached to biochips as outlined herein for the detection and quantification of metastatic colorectal cancer sequences in a particular cell. The assays are further described below in the example. PCR techniques can be used to provide greater sensitivity. Multiple protein expression monitoring can be performed as well. Similarly, these assays may be performed on an individual basis as well.

[0199] In a preferred embodiment nucleic acids encoding the metastatic colorectal cancer protein are detected. Although DNA or RNA encoding the metastatic colorectal cancer protein may be detected, of particular interest are methods wherein an mRNA encoding a metastatic colorectal cancer protein is detected. Probes to detect mRNA can be a nucleotide/deoxynucleotide probe that is complementary to and hybridizes with the mRNA and includes, but is not limited to, oligonucleotides, cDNA or RNA. Probes also should contain a detectable label, as defined herein. In one method the mRNA is detected after immobilizing the nucleic acid to be examined on a solid support such as nylon membranes and hybridizing the probe with the sample. Following washing to remove the non-specifically bound probe, the label is detected. In another method detection of the mRNA is performed in situ. In this method permeabilized cells or tissue samples are contacted with a detectably labeled nucleic acid probe for sufficient time to allow the probe to hybridize with the target mRNA. Following washing to remove the non-specifically bound probe, the label is detected. For example a digoxygenin labeled riboprobe (RNA probe) that is complementary to the mRNA encoding a metastatic colorectal cancer protein is detected by binding the digoxygenin with an anti-digoxygenin secondary antibody and developed with nitro blue tetrazolium and 5-bromo-4-chloro-3-indoyl phosphate.

[0200] In a preferred embodiment, various proteins from the three classes of proteins as described herein (secreted, transmembrane or intracellular proteins) are used in diagnostic assays. The metastatic colorectal cancer proteins, antibodies, nucleic acids, modified proteins and cells containing metastatic colorectal cancer sequences are used in diagnostic assays. This can be performed on an individual gene or corresponding polypeptide level. In a preferred embodiment, the expression profiles are used, preferably in conjunction with high throughput screening techniques to allow monitoring for expression profile genes and/or corresponding polypeptides.

[0201] As described and defined herein, metastatic colorectal cancer proteins, including intracellular, transmembrane or secreted proteins, find use as markers of metastatic colorectal cancer. Detection of these proteins in putative metastatic colorectal cancer tissue allows for detection or diagnosis of metastatic colorectal cancer. In one embodiment, antibodies are used to detect metastatic colorectal cancer proteins. A preferred method separates proteins from a sample by electrophoresis on a gel (typically a denaturing and reducing protein gel, but may be another type of gel, including isoelectric focusing gels and the like). Following separation of proteins, the metastatic colorectal cancer protein is detected, e.g., by immunoblotting with antibodies raised against the metastatic colorectal cancer protein. Methods of immunoblotting are well known to those of ordinary skill in the art.

[0202] In another preferred method, antibodies to the metastatic colorectal cancer protein find use in in situ imaging techniques, e.g., in histology (e.g., Methods in Cell Biology: Antibodies in Cell Biology, volume 37 (Asai, ed. 1993)). In this method cells are contacted with from one to many antibodies to the metastatic colorectal cancer protein(s). Following washing to remove non-specific antibody binding, the presence of the antibody or antibodies is detected. In one embodiment the antibody is detected by incubating with a secondary antibody that contains a detectable label, e.g., multicolor fluorescence or confocal imaging. In another method the primary antibody to the metastatic colorectal cancer protein(s) contains a detectable label, e.g., an enzyme marker that can act on a substrate. In another preferred embodiment each one of multiple primary antibodies contains a distinct and detectable label. This method finds particular use in simultaneous screening for a plurality of metastatic colorectal cancer proteins. Many other histological imaging techniques are also provided by the invention.

[0203] In a preferred embodiment the label is detected in a fluorometer which has the ability to detect and distinguish emissions of different wavelengths. In addition, a fluorescence activated cell sorter (FACS) can be used in the method.

[0204] In another preferred embodiment, antibodies find use in diagnosing metastatic colorectal cancer from blood, serum, plasma, stool, and other samples. Such samples, therefore, are useful as samples to be probed or tested for the presence of metastatic colorectal cancer proteins. Antibodies can be used to detect a metastatic colorectal cancer protein by previously described immunoassay techniques including ELISA, immunoblotting (western blotting), immunoprecipitation, BIACORE technology and the like. Conversely, the presence of antibodies may indicate an immune response against an endogenous metastatic colorectal cancer protein or vaccine.

[0205] In a preferred embodiment, in situ hybridization of labeled metastatic colorectal cancer nucleic acid probes to tissue arrays is done. For example, arrays of tissue samples, including metastatic colorectal cancer tissue and/or normal tissue, are made. In situ hybridization (see, e.g., Ausubel, supra) is then performed. When comparing the fingerprints between an individual and a standard, the skilled artisan can make a diagnosis, a prognosis, or a prediction based on the findings. It is further understood that the genes which indicate the diagnosis may differ from those which indicate the prognosis and molecular profiling of the condition of the cells may lead to distinctions between responsive or refractory conditions or may be predictive of outcomes.

[0206] In a preferred embodiment, the metastatic colorectal cancer proteins, antibodies, nucleic acids, modified proteins and cells containing metastatic colorectal cancer sequences are used in prognosis assays. As above, gene expression profiles can be generated that correlate to metastatic colorectal cancer, in terms of long term prognosis. Again, this may be done on either a protein or gene level, with the use of genes being preferred. As above, metastatic colorectal cancer probes may be attached to biochips for the detection and quantification of metastatic colorectal cancer sequences in a tissue or patient. The assays proceed as outlined above for diagnosis. PCR method may provide more sensitive and accurate quantification.

[0207] Assays for Therapeutic Compounds

[0208] In a preferred embodiment members of the three classes of proteins as described herein are used in drug screening assays. The metastatic colorectal cancer proteins, antibodies, nucleic acids, modified proteins and cells containing metastatic colorectal cancer sequences are used in drug screening assays or by evaluating the effect of drug candidates on a “gene expression profile” or expression profile of polypeptides. In a preferred embodiment, the expression profiles are used, preferably in conjunction with high throughput screening techniques to allow monitoring for expression profile genes after treatment with a candidate agent (e.g., Zlokarnik, et al., Science 279:84-8 (1998); Heid, Genome Res 6:986-94, 1996).

[0209] In a preferred embodiment, the metastatic colorectal cancer proteins, antibodies, nucleic acids, modified proteins and cells containing the native or modified metastatic colorectal cancer proteins are used in screening assays. That is, the present invention provides novel methods for screening for compositions which modulate the metastatic colorectal cancer phenotype or an identified physiological function of a metastatic colorectal cancer protein. As above, this can be done on an individual gene level or by evaluating the effect of drug candidates on a “gene expression profile”. In a preferred embodiment, the expression profiles are used, preferably in conjunction with high throughput screening techniques to allow monitoring for expression profile genes after treatment with a candidate agent, see Zlokarnik, supra.

[0210] Having identified the differentially expressed genes herein, a variety of assays may be applied. In a preferred embodiment, assays may be run on an individual gene or protein level. That is, having identified a particular gene with altered regulation in metastatic colorectal cancer, test compounds can be screened for the ability to modulate gene expression or for binding to the metastatic colorectal cancer protein. “Modulation” thus includes an increase or a decrease in gene expression. The preferred amount of modulation will depend on the original change of the gene expression in normal versus tissue undergoing metastatic colorectal cancer, with changes of at least 10%, preferably 50%, more preferably 100-300%, and in some embodiments 300-1000% or greater. Thus, if a gene exhibits a 4-fold increase in metastatic colorectal cancer tissue compared to normal tissue, a decrease of about four-fold is often desired; similarly, a 10-fold decrease in metastatic colorectal cancer tissue compared to normal tissue often provides a target value of a 10-fold increase in expression to be induced by the test compound.

[0211] The amount of gene expression may be monitored using nucleic acid probes and the quantification of gene expression levels, or, alternatively, the gene product itself can be monitored, e.g., through the use of antibodies to the metastatic colorectal cancer protein and standard immunoassays. Proteomics and separation techniques may also allow quantification of expression.

[0212] In a preferred embodiment, gene or protein expression monitoring of a number of entities, i.e., an expression profile, is monitored simultaneously. Such profiles will typically involve a plurality of those entities described herein.

[0213] In this embodiment, the metastatic colorectal cancer nucleic acid probes are attached to biochips as outlined herein for the detection and quantification of metastatic colorectal cancer sequences in a particular cell. Alternatively, PCR may be used. Thus, a series, e.g., of microtiter plate, may be used with dispensed primers in desired wells. A PCR reaction can then be performed and analyzed for each well.

[0214] Expression monitoring can be performed to identify compounds that modify the expression of one or more metastatic colorectal cancer-associated sequences, e.g., a polynucleotide sequence set out in Tables 1-26. Generally, in a preferred embodiment, a test compound is added to the cells prior to analysis. Moreover, screens are also provided to identify agents that modulate metastatic colorectal cancer, modulate metastatic colorectal cancer proteins, bind to a metastatic colorectal cancer protein, or interfere with the binding of a metastatic colorectal cancer protein and an antibody, substrate, or other binding partner.

[0215] The term “test compound” or “drug candidate” or “modulator” or grammatical equivalents as used herein describes any molecule, e.g., protein, oligopeptide, small organic molecule, polysaccharide, polynucleotide, etc., to be tested for the capacity to directly or indirectly alter the metastatic colorectal cancer phenotype or the expression of a metastatic colorectal cancer sequence, e.g., a nucleic acid or protein sequence. In preferred embodiments, modulators alter expression profiles of nucleic acids or proteins provided herein. In one embodiment, the modulator suppresses a metastatic colorectal cancer phenotype, e.g., to a normal tissue fingerprint. In another embodiment, a modulator induces a metastatic colorectal cancer phenotype. Generally, a plurality of assay mixtures are run in parallel with different agent concentrations to obtain a differential response to the various concentrations. Typically, one of these concentrations serves as a negative control, i.e., at zero concentration or below the level of detection.

[0216] In one aspect, a modulator will neutralize the effect of a metastatic colorectal cancer protein. By “neutralize” is meant that activity of a protein and the consequent effect on the cell is inhibited or blocked.

[0217] In certain embodiments, combinatorial libraries of potential modulators will be screened for an ability to bind to a metastatic colorectal cancer polypeptide or to modulate activity. Conventionally, new chemical entities with useful properties are generated by identifying a chemical compound (called a “lead compound”) with some desirable property or activity, e.g., inhibiting activity, creating variants of the lead compound, and evaluating the property and activity of those variant compounds. Often, high throughput screening (HTS) methods are employed for such an analysis.

[0218] In one preferred embodiment, high throughput screening methods involve providing a library containing a large number of potential therapeutic compounds (candidate compounds). Such “combinatorial chemical libraries” are then screened in one or more assays to identify those library members (particular chemical species or subclasses) that display a desired characteristic activity. The compounds thus identified can serve as conventional “lead compounds” or can themselves be used as potential or actual therapeutics.

[0219] A combinatorial chemical library is a collection of diverse chemical compounds generated by either chemical synthesis or biological synthesis by combining a number of chemical “building blocks” such as reagents. For example, a linear combinatorial chemical library, such as a polypeptide (e.g., mutein) library, is formed by combining a set of chemical building blocks called amino acids in every possible way for a given compound length (i.e., the number of amino acids in a polypeptide compound). Millions of chemical compounds can be synthesized through such combinatorial mixing of chemical building blocks (Gallop et al., J. Med. Chem. 37(9):1233-1251 (1994)).

[0220] Preparation and screening of combinatorial chemical libraries is well known to those of skill in the art. Such combinatorial chemical libraries include, but are not limited to, peptide libraries (see, e.g., U.S. Pat. No. 5,010,175, Furka, Pept. Prot. Res. 37:487-493 (1991), Houghton et al., Nature, 354:84-88 (1991)), peptoids (PCT Publication No WO 91/19735), encoded peptides (PCT Publication WO 93/20242), random bio-oligomers (PCT Publication WO 92/00091), benzodiazepines (U.S. Pat. No. 5,288,514), diversomers such as hydantoins, benzodiazepines and dipeptides (Hobbs et al., Proc. Nat. Acad. Sci. USA 90:6909-6913 (1993)), vinylogous polypeptides (Hagihara et al., J. Amer. Chem. Soc. 114:6568 (1992)), nonpeptidal peptidomimetics with a Beta-D-Glucose scaffolding (Hirschmann et al., J. Amer. Chem. Soc. 114:9217-9218 (1992)), analogous organic syntheses of small compound libraries (Chen et al., J. Amer. Chem. Soc. 116:2661 (1994)), oligocarbamates (Cho, et al., Science 261:1303 (1993)), and/or peptidyl phosphonates (Campbell et al., J. Org. Chem. 59:658 (1994)). See, generally, Gordon et al., J. Med. Chem. 37:1385 (1994), nucleic acid libraries (see, e.g., Strategene, Corp.), peptide nucleic acid libraries (see, e.g., U.S. Pat. No. 5,539,083), antibody libraries (see, e.g., Vaughn et al., Nature Biotechnology 14(3):309-314 (1996), and PCT/US96/10287), carbohydrate libraries (see, e.g., Liang et al., Science 274:1520-1522 (1996), and U.S. Pat. No. 5,593,853), and small organic molecule libraries (see, e.g., benzodiazepines, Baum, C&EN, Jan 18, page 33 (1993); isoprenoids, U.S. Pat. No. 5,569,588; thiazolidinones and metathiazanones, U.S. Pat. No. 5,549,974; pyrrolidines, U.S. Pat. Nos. 5,525,735 and 5,519,134; morpholino compounds, U.S. Pat. No. 5,506,337; benzodiazepines, U.S. Pat. No. 5,288,514; and the like).

[0221] Devices for the preparation of combinatorial libraries are commercially available (see, e.g., 357 MPS, 390 MPS, Advanced Chem Tech, Louisville Ky., Symphony, Rainin, Woburn, Mass., 433A Applied Biosystems, Foster City, Calif., 9050 Plus, Millipore, Bedford, Mass.).

[0222] A number of well known robotic systems have also been developed for solution phase chemistries. These systems include automated workstations like the automated synthesis apparatus developed by Takeda Chemical Industries, LTD. (Osaka, Japan) and many robotic systems utilizing robotic arms (Zymate II, Zymark Corporation, Hopkinton, Mass.; Orca, Hewlett-Packard, Palo Alto, Calif.), which mimic the manual synthetic operations performed by a chemist. The above devices, with appropriate modification, are suitable for use with the present invention. In addition, numerous combinatorial libraries are themselves commercially available (see, e.g., ComGenex, Princeton, N.J., Asinex, Moscow, Ru, Tripos, Inc., St. Louis, Mo., ChemStar, Ltd, Moscow, RU, 3D Pharmaceuticals, Exton, Pa., Martek Biosciences, Columbia, Md., etc.).

[0223] The assays to identify modulators are amenable to high throughput screening. Preferred assays thus detect modulation of metastatic colorectal cancer gene transcription, polypeptide expression, and polypeptide activity.

[0224] High throughput assays for evaluating the presence, absence, quantification, or other properties of particular nucleic acids or protein products are well known to those of skill in the art. Similarly, binding assays and reporter gene assays are similarly well known. Thus, e.g., U.S. Pat. No. 5,559,410 discloses high throughput screening methods for proteins, U.S. Pat. No. 5,585,639 discloses high throughput screening methods for nucleic acid binding (i.e., in arrays), while U.S. Pat. Nos. 5,576,220 and 5,541,061 disclose high throughput methods of screening for ligand/antibody binding.

[0225] In addition, high throughput screening systems are commercially available (see, e.g., Zymark Corp., Hopkinton, Mass.; Air Technical Industries, Mentor, Ohio; Beckman Instruments, Inc. Fullerton, Calif.; Precision Systems, Inc., Natick, Mass., etc.). These systems typically automate procedures, including sample and reagent pipetting, liquid dispensing, timed incubations, and final readings of the microplate in detector(s) appropriate for the assay. These configurable systems provide high throughput and rapid start up as well as a high degree of flexibility and customization. The manufacturers of such systems provide detailed protocols for various high throughput systems. Thus, e.g., Zymark Corp. provides technical bulletins describing screening systems for detecting the modulation of gene transcription, ligand binding, and the like.

[0226] In one embodiment, modulators are proteins, often naturally occurring proteins or fragments of naturally occurring proteins. Thus, e.g., cellular extracts containing proteins, or random or directed digests of proteinaceous cellular extracts, may be used. In this way libraries of proteins may be made for screening in the methods of the invention. Particularly preferred in this embodiment are libraries of bacterial, fungal, viral, and mammalian proteins, with the latter being preferred, and human proteins being especially preferred. Particularly useful test compound will be directed to the class of proteins to which the target belongs, e.g., substrates for enzymes or ligands and receptors.

[0227] In a preferred embodiment, modulators are peptides of from about 5 to about 30 amino acids, with from about 5 to about 20 amino acids being preferred, and from about 7 to about 15 being particularly preferred. The peptides may be digests of naturally occurring proteins as is outlined above, random peptides, or “biased” random peptides. By “randomized” or grammatical equivalents herein is meant that the nucleic acid or peptide consists of essentially random sequences of nucleotides and amino acids, respectively. Since these random peptides (or nucleic acids, discussed below) are often chemically synthesized, they may incorporate any nucleotide or amino acid at any position. The synthetic process can be designed to generate randomized proteins or nucleic acids, to allow the formation of all or most of the possible combinations over the length of the sequence, thus forming a library of randomized candidate bioactive proteinaceous agents.

[0228] In one embodiment, the library is fully randomized, with no sequence preferences or constants at any position. In a preferred embodiment, the library is biased. That is, some positions within the sequence are either held constant, or are selected from a limited number of possibilities. In a preferred embodiment, the nucleotides or amino acid residues are randomized within a defined class, e.g., of hydrophobic amino acids, hydrophilic residues, sterically biased (either small or large) residues, towards the creation of nucleic acid binding domains, the creation of cysteines, for cross-linking, prolines for SH-3 domains, serines, threonines, tyrosines or histidines for phosphorylation sites, etc.

[0229] Modulators of metastatic colorectal cancer can also be nucleic acids, as defined above.

[0230] As described above generally for proteins, nucleic acid modulating agents may be naturally occurring nucleic acids, random nucleic acids, or “biased” random nucleic acids. Digests of procaryotic or eucaryotic genomes may be used as is outlined above for proteins.

[0231] In a preferred embodiment, the candidate compounds are organic chemical moieties, a wide variety of which are available in the literature.

[0232] After a candidate agent has been added and the cells allowed to incubate for some period of time, the sample containing a target sequence is analyzed. If required, the target sequence is prepared using known techniques. For example, the sample may be treated to lyse the cells, using known lysis buffers, electroporation, etc., with purification and/or amplification such as PCR performed as appropriate. For example, an in vitro transcription with labels covalently attached to the nucleotides is performed. Generally, the nucleic acids are labeled with biotin-FITC or PE, or with cy3 or cy5.

[0233] In a preferred embodiment, the target sequence is labeled with, e.g., a fluorescent, a chemiluminescent, a chemical, or a radioactive signal, to provide a means of detecting the target sequence's specific binding to a probe. The label also can be an enzyme, such as, alkaline phosphatase or horseradish peroxidase, which when provided with an appropriate substrate produces a product that can be detected. Alternatively, the label can be a labeled compound or small molecule, such as an enzyme inhibitor, that binds but is not catalyzed or altered by the enzyme. The label also can be a moiety or compound, such as, an epitope tag or biotin which specifically binds to streptavidin. For the example of biotin, the streptavidin is labeled as described above, thereby, providing a detectable signal for the bound target sequence. Unbound labeled streptavidin is typically removed prior to analysis.

[0234] Nucleic acid assays can be direct hybridization assays or can comprise “sandwich assays”, which include the use of multiple probes, as is generally outlined in U.S. Pat. Nos. 5,681,702, 5,597,909, 5,545,730, 5,594,117, 5,591,584, 5,571,670, 5,580,731, 5,571,670, 5,591,584, 5,624,802, 5,635,352, 5,594,118, 5,359,100, 5,124,246 and 5,681,697, all of which are hereby incorporated by reference. In this embodiment, in general, the target nucleic acid is prepared as outlined above, and then added to the biochip comprising a plurality of nucleic acid probes, under conditions that allow the formation of a hybridization complex.

[0235] A variety of hybridization conditions may be used in the present invention, including high, moderate and low stringency conditions as outlined above. The assays are generally run under stringency conditions which allow formation of the label probe hybridization complex only in the presence of target. Stringency can be controlled by altering a step parameter that is a thermodynamic variable, including, but not limited to, temperature, formamide concentration, salt concentration, chaotropic salt concentration, pH, organic solvent concentration, etc.

[0236] These parameters may also be used to control non-specific binding, as is generally outlined in U.S. Pat. No. 5,681,697. Thus it may be desirable to perform certain steps at higher stringency conditions to reduce non-specific binding.

[0237] The reactions outlined herein may be accomplished in a variety of ways. Components of the reaction may be added simultaneously, or sequentially, in different orders, with preferred embodiments outlined below. In addition, the reaction may include a variety of other reagents. These include salts, buffers, neutral proteins, e.g., albumin, detergents, etc. which may be used to facilitate optimal hybridization and detection, and/or reduce non-specific or background interactions. Reagents that otherwise improve the efficiency of the assay, such as protease inhibitors, nuclease inhibitors, anti-microbial agents, etc., may also be used as appropriate, depending on the sample preparation methods and purity of the target.

[0238] The assay data are analyzed to determine the expression levels, and changes in expression levels as between states, of individual genes, forming a gene expression profile.

[0239] Screens are performed to identify modulators of the metastatic colorectal cancer phenotype. In one embodiment, screening is performed to identify modulators that can induce or suppress a particular expression profile, thus preferably generating the associated phenotype. In another embodiment, e.g., for diagnostic applications, having identified differentially expressed genes important in a particular state, screens can be performed to identify modulators that alter expression of individual genes. In an another embodiment, screening is performed to identify modulators that alter a biological function of the expression product of a differentially expressed gene. Again, having identified the importance of a gene in a particular state, screens are performed to identify agents that bind and/or modulate the biological activity of the gene product, or evaluate genetic polymorphisms.

[0240] Genes can be screened for those that are induced in response to a candidate agent. After identifying a modulator based upon its ability to suppress a metastatic colorectal cancer expression pattern leading to a normal expression pattern, or to modulate a single metastatic colorectal cancer gene expression profile so as to mimic the expression of the gene from normal tissue, a screen as described above can be performed to identify genes that are specifically modulated in response to the agent. Comparing expression profiles between normal tissue and agent treated metastatic colorectal cancer tissue reveals genes that are not expressed in normal tissue or metastatic colorectal cancer tissue, but are expressed in agent treated tissue. These agent-specific sequences can be identified and used by methods described herein for metastatic colorectal cancer genes or proteins. In particular these sequences and the proteins they encode find use in marking or identifying agent treated cells. In addition, antibodies can be raised against the agent induced proteins and used to target novel therapeutics to the treated metastatic colorectal cancer tissue sample.

[0241] Thus, in one embodiment, a test compound is administered to a population of metastatic colorectal cancer cells, that have an associated metastatic colorectal cancer expression profile. By “administration” or “contacting” herein is meant that the candidate agent is added to the cells in such a manner as to allow the agent to act upon the cell, whether by uptake and intracellular action, or by action at the cell surface. In some embodiments, nucleic acid encoding a proteinaceous candidate agent (i.e., a peptide) may be put into a viral construct such as an adenoviral or retroviral construct, and added to the cell, such that expression of the peptide agent is accomplished, e.g., PCT US97/01019. Regulatable gene therapy systems can also be used.

[0242] Once the test compound has been administered to the cells, the cells can be washed if desired and are allowed to incubate under preferably physiological conditions for some period of time. The cells are then harvested and a new gene expression profile is generated, as outlined herein.

[0243] Thus, e.g., metastatic colorectal cancer tissue may be screened for agents that modulate, e.g., induce or suppress the metastatic colorectal cancer phenotype. A change in at least one gene, preferably many, of the expression profile indicates that the agent has an effect on metastatic colorectal cancer activity. By defining such a signature for the metastatic colorectal cancer phenotype, screens for new drugs that alter the phenotype can be devised. With this approach, the drug target need not be known and need not be represented in the original expression screening platform, nor does the level of transcript for the target protein need to change.

[0244] Measure of metastatic colorectal cancer polypeptide activity, or of metastatic colorectal cancer or the metastatic colorectal cancer phenotype can be performed using a variety of assays. For example, the effects of the test compounds upon the function of the metastatic polypeptides can be measured by examining parameters described above. A suitable physiological change that affects activity can be used to assess the influence of a test compound on the polypeptides of this invention. When the functional consequences are determined using intact cells or animals, one can also measure a variety of effects such as, in the case of metastatic colorectal cancer associated with tumors, tumor growth, tumor metastasis, neovascularization, hormone release, transcriptional changes to both known and uncharacterized genetic markers (e.g., northern blots), changes in cell metabolism such as cell growth or pH changes, and changes in intracellular second messengers such as cGMP. In the assays of the invention, mammalian metastatic colorectal cancer polypeptide is typically used, e.g., mouse, preferably human.

[0245] Assays to identify compounds with modulating activity can be performed in vitro. For example, a colorectal cancer polypeptide is first contacted with a potential modulator and incubated for a suitable amount of time, e.g., from 0.5 to 48 hours. In one embodiment, the metastatic colorectal cancer polypeptide levels are determined in vitro by measuring the level of protein or mRNA. The level of protein is measured using immunoassays such as western blotting, ELISA and the like with an antibody that selectively binds to the metastatic colorectal cancer polypeptide or a fragment thereof. For measurement of mRNA, amplification, e.g., using PCR, LCR, or hybridization assays, e.g., northern hybridization, RNAse protection, dot blotting, are preferred. The level of protein or mRNA is detected using directly or indirectly labeled detection agents, e.g., fluorescently or radioactively labeled nucleic acids, radioactively or enzymatically labeled antibodies, and the like, as described herein.

[0246] Alternatively, a reporter gene system can be devised using the metastatic colorectal cancer protein promoter operably linked to a reporter gene such as luciferase, green fluorescent protein, CAT, or β-gal. The reporter construct is typically transfected into a cell. After treatment with a potential modulator, the amount of reporter gene transcription, translation, or activity is measured according to standard techniques known to those of skill in the art.

[0247] In a preferred embodiment, as outlined above, screens may be done on individual genes and gene products (proteins). That is, having identified a particular differentially expressed gene as important in a particular state, screening of modulators of the expression of the gene or the gene product itself can be done. The gene products of differentially expressed genes are sometimes referred to herein as “metastatic colorectal cancer proteins.” The metastatic colorectal cancer protein may be a fragment, or alternatively, be the full length protein to a fragment shown herein.

[0248] In one embodiment, screening for modulators of expression of specific genes is performed. Typically, the expression of only one or a few genes are evaluated. In another embodiment, screens are designed to first find compounds that bind to differentially expressed proteins. These compounds are then evaluated for the ability to modulate differentially expressed activity. Moreover, once initial candidate compounds are identified, variants can be further screened to better evaluate structure activity relationships.

[0249] In a preferred embodiment, binding assays are done. In general, purified or isolated gene product is used; that is, the gene products of one or more differentially expressed nucleic acids are made. For example, antibodies are generated to the protein gene products, and standard immunoassays are run to determine the amount of protein present. Alternatively, cells comprising the metastatic colorectal cancer proteins can be used in the assays.

[0250] Thus, in a preferred embodiment, the methods comprise combining a metastatic colorectal cancer protein and a candidate compound, and determining the binding of the compound to the metastatic colorectal cancer protein. Preferred embodiments utilize the human metastatic colorectal cancer protein, although other mammalian proteins may also be used, e.g., for the development of animal models of human disease. In some embodiments, as outlined herein, variant or derivative metastatic colorectal cancer proteins may be used.

[0251] Generally, in a preferred embodiment of the methods herein, the metastatic colorectal cancer protein or the candidate agent is non-diffusably bound to an insoluble support having isolated sample receiving areas (e.g., a microtiter plate, an array, etc.). The insoluble supports may be made of any composition to which the compositions can be bound, is readily separated from soluble material, and is otherwise compatible with the overall method of screening. The surface of such supports may be solid or porous and of any convenient shape. Examples of suitable insoluble supports include microtiter plates, arrays, membranes and beads. These are typically made of glass, plastic (e.g., polystyrene), polysaccharides, nylon or nitrocellulose, teflon™, etc. Microtiter plates and arrays are especially convenient because a large number of assays can be carried out simultaneously, using small amounts of reagents and samples. The particular manner of binding of the composition is not crucial so long as it is compatible with the reagents and overall methods of the invention, maintains the activity of the composition and is nondiffusable. Preferred methods of binding include the use of antibodies (which do not sterically block either the ligand binding site or activation sequence when the protein is bound to the support), direct binding to “sticky” or ionic supports, chemical crosslinking, the synthesis of the protein or agent on the surface, etc. Following binding of the protein or agent, excess unbound material is removed by washing. The sample receiving areas may then be blocked through incubation with bovine serum albumin (BSA), casein or other innocuous protein or other moiety.

[0252] In a preferred embodiment, the metastatic colorectal cancer protein is bound to the support, and a test compound is added to the assay. Alternatively, the candidate agent is bound to the support and the metastatic colorectal cancer protein is added. Novel binding agents include specific antibodies, non-natural binding agents identified in screens of chemical libraries, peptide analogs, etc. Of particular interest are screening assays for agents that have a low toxicity for human cells. A wide variety of assays may be used for this purpose, including labeled in vitro protein-protein binding assays, electrophoretic mobility shift assays, immunoassays for protein binding, functional assays (phosphorylation assays, etc.) and the like.

[0253] The determination of the binding of the test modulating compound to the metastatic colorectal cancer protein may be done in a number of ways. In a preferred embodiment, the compound is labeled, and binding determined directly, e.g., by attaching all or a portion of the metastatic colorectal cancer protein to a solid support, adding a labeled candidate agent (e.g., a fluorescent label), washing off excess reagent, and determining whether the label is present on the solid support. Various blocking and washing steps may be utilized as appropriate.

[0254] In some embodiments, only one of the components is labeled, e.g., the proteins (or proteinaceous candidate compounds) can be labeled. Alternatively, more than one component can be labeled with different labels, e.g., ¹²⁵I for the proteins and a fluorophor for the compound. Proximity reagents, e.g., quenching or energy transfer reagents are also useful.

[0255] In one embodiment, the binding of the test compound is determined by competitive binding assay. The competitor is a binding moiety known to bind to the target molecule (i.e., a metastatic colorectal cancer protein), such as an antibody, peptide, binding partner, ligand, etc. Under certain circumstances, there may be competitive binding between the compound and the binding moiety, with the binding moiety displacing the compound. In one embodiment, the test compound is labeled. Either the compound, or the competitor, or both, is added first to the protein for a time sufficient to allow binding, if present. Incubations may be performed at a temperature which facilitates optimal activity, typically between 4 and 40° C. Incubation periods are typically optimized, e.g., to facilitate rapid high throughput screening. Typically between 0.1 and 1 hour will be sufficient. Excess reagent is generally removed or washed away. The second component is then added, and the presence or absence of the labeled component is followed, to indicate binding.

[0256] In a preferred embodiment, the competitor is added first, followed by the test compound. Displacement of the competitor is an indication that the test compound is binding to the metastatic colorectal cancer protein and thus is capable of binding to, and potentially modulating, the activity of the metastatic colorectal cancer protein. In this embodiment, either component can be labeled. Thus, e.g., if the competitor is labeled, the presence of label in the wash solution indicates displacement by the agent. Alternatively, if the test compound is labeled, the presence of the label on the support indicates displacement.

[0257] In an alternative embodiment, the test compound is added first, with incubation and washing, followed by the competitor. The absence of binding by the competitor may indicate that the test compound is bound to the metastatic colorectal cancer protein with a higher affinity. Thus, if the test compound is labeled, the presence of the label on the support, coupled with a lack of competitor binding, may indicate that the test compound is capable of binding to the metastatic colorectal cancer protein.

[0258] In a preferred embodiment, the methods comprise differential screening to identity agents that are capable of modulating the activity of the metastatic colorectal cancer proteins. In this embodiment, the methods comprise combining a metastatic colorectal cancer protein and a competitor in a first sample. A second sample comprises a test compound, a metastatic colorectal cancer protein, and a competitor. The binding of the competitor is determined for both samples, and a change, or difference in binding between the two samples indicates the presence of an agent capable of binding to the metastatic colorectal cancer protein and potentially modulating its activity. That is, if the binding of the competitor is different in the second sample relative to the first sample, the agent is capable of binding to the metastatic colorectal cancer protein.

[0259] Alternatively, differential screening is used to identify drug candidates that bind to the native metastatic colorectal cancer protein, but cannot bind to modified metastatic colorectal cancer proteins. The structure of the metastatic colorectal cancer protein may be modeled, and used in rational drug design to synthesize agents that interact with that site. Drug candidates that affect the activity of a metastatic colorectal cancer protein are also identified by screening drugs for the ability to either enhance or reduce the activity of the protein.

[0260] Positive controls and negative controls may be used in the assays. Preferably control and test samples are performed in at least triplicate to obtain statistically significant results. Incubation of all samples is for a time sufficient for the binding of the agent to the protein. Following incubation, samples are washed free of non-specifically bound material and the amount of bound, generally labeled agent determined. For example, where a radiolabel is employed, the samples may be counted in a scintillation counter to determine the amount of bound compound.

[0261] A variety of other reagents may be included in the screening assays. These include reagents like salts, neutral proteins, e.g., albumin, detergents, etc. which may be used to facilitate optimal protein-protein binding and/or reduce non-specific or background interactions. Also reagents that otherwise improve the efficiency of the assay, such as protease inhibitors, nuclease inhibitors, anti-microbial agents, etc., may be used. The mixture of components may be added in an order that provides for the requisite binding.

[0262] In a preferred embodiment, the invention provides methods for screening for a compound capable of modulating the activity of a metastatic colorectal cancer protein. The methods comprise adding a test compound, as defined above, to a cell comprising metastatic colorectal cancer proteins. Preferred cell types include almost any cell. The cells contain a recombinant nucleic acid that encodes a metastatic colorectal cancer protein. In a preferred embodiment, a library of candidate agents are tested on a plurality of cells.

[0263] In one aspect, the assays are evaluated in the presence or absence or previous or subsequent exposure of physiological signals, e.g., hormones, antibodies, peptides, antigens, cytokines, growth factors, action potentials, pharmacological agents including chemotherapeutics, radiation, carcinogenics, or other cells (i.e. cell-cell contacts). In another example, the determinations are determined at different stages of the cell cycle process.

[0264] In this way, compounds that modulate metastatic colorectal cancer agents are identified. Compounds with pharmacological activity are able to enhance or interfere with the activity of the metastatic colorectal cancer protein. Once identified, similar structures are evaluated to identify critical structural feature of the compound.

[0265] In one embodiment, a method of inhibiting metastatic colorectal cancer cell division is provided. The method comprises administration of a metastatic colorectal cancer inhibitor. In another embodiment, a method of inhibiting metastatic colorectal cancer is provided. The method comprises administration of a metastatic colorectal cancer inhibitor. In a further embodiment, methods of treating cells or individuals with metastatic colorectal cancer are provided. The method comprises administration of a metastatic colorectal cancer inhibitor.

[0266] A variety of cell growth, proliferation, and metastasis assays are known to those of skill in the art, as described below.

[0267] Soft Agar Growth or Colony Formation in Suspension

[0268] Normal cells require a solid substrate to attach and grow. When the cells are transformed, they lose this phenotype and grow detached from the substrate. For example, transformed cells can grow in stirred suspension culture or suspended in semi-solid media, such as semi-solid or soft agar. The transformed cells, when transfected with tumor suppressor genes, regenerate normal phenotype and require a solid substrate to attach and grow. Soft agar growth or colony formation in suspension assays can be used to identify modulators of metastatic colorectal cancer sequences, which when expressed in host cells, inhibit abnormal cellular proliferation and transformation. A therapeutic compound would reduce or eliminate the host cells' ability to grow in stirred suspension culture or suspended in semi-solid media, such as semi-solid or soft.

[0269] Techniques for soft agar growth or colony formation in suspension assays are described in Freshney, Culture of Animal Cells a Manual of Basic Technique (3^(rd) ed., 1994), herein incorporated by reference. See also, the methods section of Garkavtsev et al. (1996), supra, herein incorporated by reference.

[0270] Contact Inhibition and Density Limitation of Growth

[0271] Normal cells typically grow in a flat and organized pattern in a petri dish until they touch other cells. When the cells touch one another, they are contact inhibited and stop growing. When cells are transformed, however, the cells are not contact inhibited and continue to grow to high densities in disorganized foci. Thus, the transformed cells grow to a higher saturation density than normal cells. This can be detected morphologically by the formation of a disoriented monolayer of cells or rounded cells in foci within the regular pattern of normal surrounding cells. Alternatively, labeling index with (³H)-thymidine at saturation density can be used to measure density limitation of growth. See Freshney (1994), supra. The transformed cells, when transfected with tumor suppressor genes, regenerate a normal phenotype and become contact inhibited and would grow to a lower density.

[0272] In this assay, labeling index with (³H)-thymidine at saturation density is a preferred method of measuring density limitation of growth. Transformed host cells are transfected with a metastatic colorectal cancer-associated sequence and are grown for 24 hours at saturation density in non-limiting medium conditions. The percentage of cells labeling with (³H)-thymidine is determined autoradiographically. See, Freshney (1994), supra.

[0273] Growth Factor or Serum Dependence

[0274] Transformed cells have a lower serum dependence than their normal counterparts (see, e.g., Temin, J. Natl. Cancer Insti. 37:167-175 (1966); Eagle et al., J. Exp. Med. 131:836-879 (1970)); Freshney, supra. This is in part due to release of various growth factors by the transformed cells. Growth factor or serum dependence of transformed host cells can be compared with that of control.

[0275] Tumor Specific Markers Levels

[0276] Tumor cells release an increased amount of certain factors (hereinafter “tumor specific markers”) than their normal counterparts. For example, plasminogen activator (PA) is released from human glioma at a higher level than from normal brain cells (see, e.g., Gullino, Angiogenesis, tumor vascularization, and potential interference with tumor growth. in Biological Responses in Cancer, pp. 178-184 (Mihich (ed.) 1985)). Similarly, Tumor angiogenesis factor (TAF) is released at a higher level in tumor cells than their normal counterparts. See, e.g., Folkman, Angiogenesis and Cancer, Sem Cancer Biol. (1992)).

[0277] Various techniques which measure the release of these factors are described in Freshney (1994), supra. Also, see, Unkless et al., J. Biol. Chem. 249:4295-4305 (1974); Strickland & Beers, J. Biol. Chem. 251:5694-5702 (1976); Whur et al., Br. J. Cancer 42:305-312 (1980); Gullino, Angiogenesis, tumor vascularization, and potential interference with tumor growth. in Biological Responses in Cancer, pp. 178-184 (Mihich (ed.) 1985); Freshney Anticancer Res. 5:111-130 (1985).

[0278] Invasiveness Into Matrigel

[0279] The degree of invasiveness into Matrigel or some other extracellular matrix constituent can be used as an assay to identify compounds that modulate metastatic colorectal cancer-associated sequences. Tumor cells exhibit a good correlation between malignancy and invasiveness of cells into Matrigel or some other extracellular matrix constituent. In this assay, tumorigenic cells are typically used as host cells. Expression of a tumor suppressor gene in these host cells would decrease invasiveness of the host cells.

[0280] Techniques described in Freshney (1994), supra, can be used. Briefly, the level of invasion of host cells can be measured by using filters coated with Matrigel or some other extracellular matrix constituent. Penetration into the gel, or through to the distal side of the filter, is rated as invasiveness, and rated histologically by number of cells and distance moved, or by prelabeling the cells with ¹²⁵I and counting the radioactivity on the distal side of the filter or bottom of the dish. See, e.g., Freshney (1984), supra.

[0281] Tumor Growth in vivo

[0282] Effects of metastatic colorectal cancer-associated sequences on cell growth can be tested in transgenic or immune-suppressed mice. Knock-out transgenic mice can be made, in which the metastatic colorectal cancer gene is disrupted or in which a metastatic colorectal cancer gene is inserted. Knock-out transgenic mice can be made by insertion of a marker gene or other heterologous gene into the endogenous metastatic colorectal cancer gene site in the mouse genome via homologous recombination. Such mice can also be made by substituting the endogenous metastatic colorectal cancer gene with a mutated version of the metastatic colorectal cancer gene, or by mutating the endogenous metastatic colorectal cancer gene, e.g., by exposure to carcinogens.

[0283] A DNA construct is introduced into the nuclei of embryonic stem cells. Cells containing the newly engineered genetic lesion are injected into a host mouse embryo, which is re-implanted into a recipient female. Some of these embryos develop into chimeric mice that possess germ cells partially derived from the mutant cell line. Therefore, by breeding the chimeric mice it is possible to obtain a new line of mice containing the introduced genetic lesion (see, e.g., Capecchi et al., Science 244:1288 (1989)). Chimeric targeted mice can be derived according to Hogan et al., Manipulating the Mouse Embryo: A Laboratory Manual, Cold Spring Harbor Laboratory (1988) and Teratocarcinomas and Embryonic Stem Cells: A Practical Approach, Robertson, ed., IRL Press, Washington, D.C., (1987).

[0284] Alternatively, various immune-suppressed or immune-deficient host animals can be used. For example, genetically athymic “nude” mouse (see, e.g., Giovanella et al., J. Natl. Cancer Inst. 52:921 (1974)), a SCID mouse, a thymectomized mouse, or an irradiated mouse (see, e.g., Bradley et al., Br. J. Cancer 38:263 (1978); Selby et al., Br. J. Cancer 41:52 (1980)) can be used as a host. Transplantable tumor cells (typically about 10⁶ cells) injected into isogenic hosts will produce invasive tumors in a high proportions of cases, while normal cells of similar origin will not. In hosts which developed invasive tumors, cells expressing a metastatic colorectal cancer-associated sequences are injected subcutaneously. After a suitable length of time, preferably 4-8 weeks, tumor growth is measured (e.g., by volume or by its two largest dimensions) and compared to the control. Tumors that have statistically significant reduction (using, e.g., Student's T test) are said to have inhibited growth. Additionally, human tumor cells expressing the genes of the invention may be injected into immune compromised animals. Growth of these tumors, or xenografts, is compared to growth of similar human tumor cell that do not express the genes of the invention. These animals may also be used to binding assays and efficacy studies for therapeutic compounds that modulate metastatic colorectal cancer, such as antibodies or small molecules.

[0285] Polynucleotide Modulators of Metastatic Colorectal Cancer

[0286] Antisense Polynucleotides

[0287] In certain embodiments, the activity of a metastatic colorectal cancer-associated protein is downregulated, or entirely inhibited, by the use of antisense polynucleotide, i.e., a nucleic acid complementary to, and which can preferably hybridize specifically to, a coding mRNA nucleic acid sequence, e.g., a metastatic colorectal cancer protein mRNA, or a subsequence thereof. Binding of the antisense polynucleotide to the mRNA reduces the translation and/or stability of the mRNA.

[0288] In the context of this invention, antisense polynucleotides can comprise naturally-occurring nucleotides, or synthetic species formed from naturally-occurring subunits or their close homologs. Antisense polynucleotides may also have altered sugar moieties or inter-sugar linkages. Exemplary among these are the phosphorothioate and other sulfur containing species which are known for use in the art. Analogs are comprehended by this invention so long as they function effectively to hybridize with the metastatic colorectal cancer protein mRNA. See, e.g., Isis Pharmaceuticals, Carlsbad, Calif.; Sequitor, Inc., Natick, Mass.

[0289] Such antisense polynucleotides can readily be synthesized using recombinant means, or can be synthesized in vitro. Equipment for such synthesis is sold by several vendors, including Applied Biosystems. The preparation of other oligonucleotides such as phosphorothioates and alkylated derivatives is also well known to those of skill in the art.

[0290] Antisense molecules as used herein include antisense or sense oligonucleotides. Sense oligonucleotides can, e.g., be employed to block transcription by binding to the anti-sense strand. The antisense and sense oligonucleotide comprise a single-stranded nucleic acid sequence (either RNA or DNA) capable of binding to target mRNA (sense) or DNA (antisense) sequences for metastatic colorectal cancer molecules. A preferred antisense molecule is for a metastatic colorectal cancer sequence in Tables 1-26, or for a ligand or activator thereof. Antisense or sense oligonucleotides, according to the present invention, comprise a fragment generally at least about 14 nucleotides, preferably from about 14 to 30 nucleotides. The ability to derive an antisense or a sense oligonucleotide, based upon a cDNA sequence encoding a given protein is described in, e.g., Stein & Cohen (Cancer Res. 48:2659 (1988 and van der Krol et al. (BioTechniques 6:958 (1988)).

[0291] Ribozymes

[0292] In addition to antisense polynucleotides, ribozymes can be used to target and inhibit transcription of metastatic colorectal cancer-associated nucleotide sequences. A ribozyme is an RNA molecule that catalytically cleaves other RNA molecules. Different kinds of ribozymes have been described, including group I ribozymes, hammerhead ribozymes, hairpin ribozymes, RNase P, and axhead ribozymes (see, e.g., Castanotto et al., Adv. in Pharmacology 25: 289-317 (1994) for a general review of the properties of different ribozymes).

[0293] The general features of hairpin ribozymes are described, e.g., in Hampel et al., Nucl. Acids Res. 18:299-304 (1990); European Patent Publication No. 0 360 257; U.S. Pat. No. 5,254,678. Methods of preparing are well known to those of skill in the art (see, e.g., WO 94/26877; Ojwang et al., Proc. Natl. Acad. Sci. USA 90:6340-6344 (1993); Yamada et al., Human Gene Therapy 1:39-45 (1994); Leavitt et al., Proc. Natl. Acad. Sci. USA 92:699-703 (1995); Leavitt et al., Human Gene Therapy 5:1151-120 (1994); and Yamada et al., Virology 205: 121-126 (1994)).

[0294] Polynucleotide modulators of metastatic colorectal cancer may be introduced into a cell containing the target nucleotide sequence by formation of a conjugate with a ligand binding molecule, as described in WO 91/04753. Suitable ligand binding molecules include, but are not limited to, cell surface receptors, growth factors, other cytokines, or other ligands that bind to cell surface receptors. Preferably, conjugation of the ligand binding molecule does not substantially interfere with the ability of the ligand binding molecule to bind to its corresponding molecule or receptor, or block entry of the sense or antisense oligonucleotide or its conjugated version into the cell. Alternatively, a polynucleotide modulator of metastatic colorectal cancer may be introduced into a cell containing the target nucleic acid sequence, e.g., by formation of an polynucleotide-lipid complex, as described in WO 90/10448. It is understood that the use of antisense molecules or knock out and knock in models may also be used in screening assays as discussed above, in addition to methods of treatment.

[0295] Thus, in one embodiment, methods of modulating metastatic colorectal cancer in cells or organisms are provided. In one embodiment, the methods comprise administering to a cell an anti-metastatic colorectal cancer antibody that reduces or eliminates the biological activity of an endogenous metastatic colorectal cancer protein. Alternatively, the methods comprise administering to a cell or organism a recombinant nucleic acid encoding a metastatic colorectal cancer protein. This may be accomplished in any number of ways. In a preferred embodiment, e.g., when the metastatic colorectal cancer sequence is down-regulated in metastatic colorectal cancer, such state may be reversed by increasing the amount of metastatic colorectal cancer gene product in the cell. This can be accomplished, e.g., by overexpressing the endogenous metastatic colorectal cancer gene or administering a gene encoding the metastatic colorectal cancer sequence, using known gene-therapy techniques. In a preferred embodiment, the gene therapy techniques include the incorporation of the exogenous gene using enhanced homologous recombination (EHR), e.g., as described in PCT/US93/03868, hereby incorporated by reference in its entirety. Alternatively, e.g., when the metastatic colorectal cancer sequence is up-regulated in metastatic colorectal cancer, the activity of the endogenous metastatic colorectal cancer gene is decreased, e.g., by the administration of a metastatic colorectal cancer antisense nucleic acid.

[0296] In one embodiment, the metastatic colorectal cancer proteins of the present invention may be used to generate polyclonal and monoclonal antibodies to metastatic colorectal cancer proteins. Similarly, the metastatic colorectal cancer proteins can be coupled, using standard technology, to affinity chromatography columns. These columns may then be used to purify metastatic colorectal cancer antibodies useful for production, diagnostic, or therapeutic purposes. In a preferred embodiment, the antibodies are generated to epitopes unique to a metastatic colorectal cancer protein; that is, the antibodies show little or no cross-reactivity to other proteins. The metastatic colorectal cancer antibodies may be coupled to standard affinity chromatography columns and used to purify metastatic colorectal cancer proteins. The antibodies may also be used as blocking polypeptides, as outlined above, since they will specifically bind to the metastatic colorectal cancer protein.

[0297] Methods of Identifying Variant Metastatic Colorectal Cancer-Associated Sequences

[0298] Without being bound by theory, expression of various metastatic colorectal cancer sequences is correlated with metastatic colorectal cancer. Accordingly, disorders based on mutant or variant metastatic colorectal cancer genes may be determined. In one embodiment, the invention provides methods for identifying cells containing variant metastatic colorectal cancer genes, e.g., determining all or part of the sequence of at least one endogenous metastatic colorectal cancer genes in a cell. This may be accomplished using any number of sequencing techniques. In a preferred embodiment, the invention provides methods of identifying the metastatic colorectal cancer genotype of an individual, e.g., determining all or part of the sequence of at least one metastatic colorectal cancer gene of the individual. This is generally done in at least one tissue of the individual, and may include the evaluation of a number of tissues or different samples of the same tissue. The method may include comparing the sequence of the sequenced metastatic colorectal cancer gene to a known metastatic colorectal cancer gene, i.e., a wild-type gene.

[0299] The sequence of all or part of the metastatic colorectal cancer gene can then be compared to the sequence of a known metastatic colorectal cancer gene to determine if any differences exist. This can be done using any number of known homology programs, such as Bestfit, etc. In a preferred embodiment, the presence of a difference in the sequence between the metastatic colorectal cancer gene of the patient and the known metastatic colorectal cancer gene correlates with a disease state or a propensity for a disease state, as outlined herein.

[0300] In a preferred embodiment, the metastatic colorectal cancer genes are used as probes to determine the number of copies of the metastatic colorectal cancer gene in the genome.

[0301] In another preferred embodiment, the metastatic colorectal cancer genes are used as probes to determine the chromosomal localization of the metastatic colorectal cancer genes. Information such as chromosomal localization finds use in providing a diagnosis or prognosis in particular when chromosomal abnormalities such as translocations, and the like are identified in the metastatic colorectal cancer gene locus.

[0302] Administration of Pharmaceutical and Vaccine Compositions

[0303] In one embodiment, a therapeutically effective dose of a metastatic colorectal cancer protein or modulator thereof, is administered to a patient. By “therapeutically effective dose” herein is meant a dose that produces effects for which it is administered. The exact dose will depend on the purpose of the treatment, and will be ascertainable by one skilled in the art using known techniques (e.g., Ansel et al., Pharmaceutical Dosage Forms and Drug Delivery; Lieberman, Pharmaceutical Dosage Forms (vols. 1-3, 1992), Dekker, ISBN 0824770846, 082476918X, 0824712692, 0824716981; Lloyd, The Art, Science and Technology of Pharmaceutical Compounding (1999); and Pickar, Dosage Calculations (1999)). As is known in the art, adjustments for metastatic colorectal cancer degradation, systemic versus localized delivery, and rate of new protease synthesis, as well as the age, body weight, general health, sex, diet, time of administration, drug interaction and the severity of the condition may be necessary, and will be ascertainable with routine experimentation by those skilled in the art.

[0304] A “patient” for the purposes of the present invention includes both humans and other animals, particularly mammals. Thus the methods are applicable to both human therapy and veterinary applications. In the preferred embodiment the patient is a mammal, preferably a primate, and in the most preferred embodiment the patient is human.

[0305] The administration of the metastatic colorectal cancer proteins and modulators thereof of the present invention can be done in a variety of ways as discussed above, including, but not limited to, orally, subcutaneously, intravenously, intranasally, transdermally, intraperitoneally, intramuscularly, intrapulmonary, vaginally, rectally, or intraocularly. In some instances, e.g., in the treatment of wounds and inflammation, the metastatic colorectal cancer proteins and modulators may be directly applied as a solution or spray.

[0306] The pharmaceutical compositions of the present invention comprise a metastatic colorectal cancer protein in a form suitable for administration to a patient. In the preferred embodiment, the pharmaceutical compositions are in a water soluble form, such as being present as pharmaceutically acceptable salts, which is meant to include both acid and base addition salts. “Pharmaceutically acceptable acid addition salt” refers to those salts that retain the biological effectiveness of the free bases and that are not biologically or otherwise undesirable, formed with inorganic acids such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid and the like, and organic acids such as acetic acid, propionic acid, glycolic acid, pyruvic acid, oxalic acid, maleic acid, malonic acid, succinic acid, fumaric acid, tartaric acid, citric acid, benzoic acid, cinnamic acid, mandelic acid, methanesulfonic acid, ethanesulfonic acid, p-toluenesulfonic acid, salicylic acid and the like. “Pharmaceutically acceptable base addition salts” include those derived from inorganic bases such as sodium, potassium, lithium, ammonium, calcium, magnesium, iron, zinc, copper, manganese, aluminum salts and the like. Particularly preferred are the ammonium, potassium, sodium, calcium, and magnesium salts. Salts derived from pharmaceutically acceptable organic non-toxic bases include salts of primary, secondary, and tertiary amines, substituted amines including naturally occurring substituted amines, cyclic amines and basic ion exchange resins, such as isopropylamine, trimethylamine, diethylamine, triethylamine, tripropylamine, and ethanolamine.

[0307] The pharmaceutical compositions may also include one or more of the following: carrier proteins such as serum albumin; buffers; fillers such as microcrystalline cellulose, lactose, corn and other starches; binding agents; sweeteners and other flavoring agents; coloring agents; and polyethylene glycol.

[0308] The pharmaceutical compositions can be administered in a variety of unit dosage forms depending upon the method of administration. For example, unit dosage forms suitable for oral administration include, but are not limited to, powder, tablets, pills, capsules and lozenges. It is recognized that metastatic colorectal cancer protein modulators (e.g., antibodies, antisense constructs, ribozymes, small organic molecules, etc.) when administered orally, should be protected from digestion. It is also recognized that, after delivery to other sites in the body (e.g., circulatory system, lymphatic system, or the tumor site) the metastatic colorectal cancer modulators of the invention may need to be protected from excretion, hydrolisis, proteolytic digestion or modification, or detoxification by the liver. In all these cases, protection is typically accomplished either by complexing the molecule(s) with a composition to render it resistant to acidic and enzymatic hydrolysis, or by packaging the molecule(s) in an appropriately resistant carrier, such as a liposome or a protection barrier or by modifying the molecular size, weight, and/or charge of the modulator. Means of protecting agents from digestion degradation, and excretion are well known in the art.

[0309] The compositions for administration will commonly comprise a metastatic colorectal cancer protein modulator dissolved in a pharmaceutically acceptable carrier, preferably an aqueous carrier. A variety of aqueous carriers can be used, e.g., buffered saline and the like. These solutions are sterile and generally free of undesirable matter. These compositions may be sterilized by conventional, well known sterilization techniques. The compositions may contain pharmaceutically acceptable auxiliary substances as required to approximate physiological conditions such as pH adjusting and buffering agents, toxicity adjusting agents and the like, e.g., sodium acetate, sodium chloride, potassium chloride, calcium chloride, sodium lactate and the like. The concentration of active agent in these formulations can vary widely, and will be selected primarily based on fluid volumes, viscosities, body weight and the like in accordance with the particular mode of administration selected and the patient's needs (e.g., Remington's Pharmaceutical Science (15th ed., 1980) and Goodman & Gillman, The Pharmacologial Basis of Therapeutics (Hardman et al., eds., 1996)).

[0310] Thus, a typical pharmaceutical composition for intravenous administration would be about 0.1 to 10 mg per patient per day. Dosages from 0.1 up to about 100 mg per patient per day may be used, particularly when the drug is administered to a secluded site and not into the blood stream, such as into a body cavity or into a lumen of an organ. Substantially higher dosages are possible in topical administration. Actual methods for preparing parenterally administrable compositions will be known or apparent to those skilled in the art, e.g., Remington 's Pharmaceutical Science and Goodman and Gilhman, The Pharmacologial Basis of Therapeutics, supra.

[0311] The compositions containing modulators of metastatic colorectal cancer proteins can be administered for therapeutic or prophylactic treatments. In therapeutic applications, compositions are administered to a patient suffering from a disease (e.g., a cancer) in an amount sufficient to cure or at least partially arrest the disease and its complications. An amount adequate to accomplish this is defined as a “therapeutically effective dose.” Amounts effective for this use will depend upon the severity of the disease and the general state of the patient's health. Single or multiple administrations of the compositions may be administered depending on the dosage and frequency as required and tolerated by the patient. In any event, the composition should provide a sufficient quantity of the agents of this invention to effectively treat the patient. An amount of modulator that is capable of preventing or slowing the development of cancer in a mammal is referred to as a “prophylactically effective dose.” The particular dose required for a prophylactic treatment will depend upon the medical condition and history of the mammal, the particular cancer being prevented, as well as other factors such as age, weight, gender, administration route, efficiency, etc. Such prophylactic treatments may be used, e.g., in a mammal who has previously had cancer to prevent a recurrence of the cancer, or in a mammal who is suspected of having a significant likelihood of developing cancer.

[0312] It will be appreciated that the present metastatic colorectal cancer protein-modulating compounds can be administered alone or in combination with additional metastatic colorectal cancer modulating compounds or with other therapeutic agent, e.g., other anti-cancer agents or treatments.

[0313] In numerous embodiments, one or more nucleic acids, e.g., polynucleotides comprising nucleic acid sequences set forth in Tables 1-26, such as antisense polynucleotides or ribozymes, will be introduced into cells, in vitro or in vivo. The present invention provides methods, reagents, vectors, and cells useful for expression of metastatic colorectal cancer-associated polypeptides and nucleic acids using in vitro (cell-free), ex vivo or in vivo (cell or organism-based) recombinant expression systems.

[0314] The particular procedure used to introduce the nucleic acids into a host cell for expression of a protein or nucleic acid is application specific. Many procedures for introducing foreign nucleotide sequences into host cells may be used. These include the use of calcium phosphate transfection, spheroplasts, electroporation, liposomes, microinjection, plasma vectors, viral vectors and any of the other well known methods for introducing cloned genomic DNA, cDNA, synthetic DNA or other foreign genetic material into a host cell (see, e.g., Berger & Kimmel, Guide to Molecular Cloning Techniques, Methods in Enzymology volume 152 (Berger), Ausubel et al., eds., Current Protocols (supplemented through 1999), and Sambrook et al., Molecular Cloning—A Laboratory Manual (2nd ed., Vol. 1-3, 1989.

[0315] In a preferred embodiment, metastatic colorectal cancer proteins and modulators are administered as therapeutic agents, and can be formulated as outlined above. Similarly, metastatic colorectal cancer genes (including both the full-length sequence, partial sequences, or regulatory sequences of the metastatic colorectal cancer coding regions) can be administered in a gene therapy application. These metastatic colorectal cancer genes can include antisense applications, either as gene therapy (i.e., for incorporation into the genome) or as antisense compositions, as will be appreciated by those in the art.

[0316] Metastatic colorectal cancer polypeptides and polynucleotides can also be administered as vaccine compositions to stimulate HTL, CTL and antibody responses. Such vaccine compositions can include, e.g., lipidated peptides (see, e.g., Vitiello, et al., J. Clin. Invest. 95:341 (1995)), peptide compositions encapsulated in poly(DL-lactide-co-glycolide) (“PLG”) microspheres (see, e.g., Eldridge, et al., Molec. Immunol. 28:287-294, (1991); Alonso et al., Vaccine 12:299-306 (1994); Jones et al., Vaccine 13:675-681 (1995)), peptide compositions contained in immune stimulating complexes (ISCOMS) (see, e.g., Takahashi et al., Nature 344:873-875 (1990); Hu et al., Clin Exp Immunol. 113:235-243 (1998)), multiple antigen peptide systems (MAPs) (see, e.g., Tam, Proc. Natl. Acad. Sci. U.S.A. 85:5409-5413 (1988); Tam, J. Immunol. Methods 196:17-32 (1996)), peptides formulated as multivalent peptides; peptides for use in ballistic delivery systems, typically crystallized peptides, viral delivery vectors (Perkus, et al., In: Concepts in vaccine development (Kaufmann, ed., p. 379, 1996); Chakrabarti, et al., Nature 320:535 (1986); Hu et al., Nature 320:537 (1986); Kieny, et al., AIDS Bio/Technology 4:790 (1986); Top et al., J. Infect. Dis. 124:148 (1971); Chanda et al., Virology 175:535 (1990)), particles of viral or synthetic origin (see, e.g., Kofler et al., J. Immunol. Methods. 192:25 (1996); Eldridge et al., Sem. Hematol. 30:16 (1993); Falo et al., Nature Med. 7:649 (1995)), adjuvants (Warren et al., Annu. Rev. Immunol. 4:369 (1986); Gupta et al., Vaccine 11:293 (1993)), liposomes (Reddy et al., J. Immunol. 148:1585 (1992); Rock, Immunol. Today 17:131 (1996)), or, naked or particle absorbed cDNA (Ulmer, et al., Science 259:1745 (1993); Robinson et al., Vaccine 11:957 (1993); Shiver et al., In: Concepts in vaccine development (Kaufmann, ed., p. 423, 1996); Cease & Berzofsky, Annu. Rev. Immunol. 12:923 (1994) and Eldridge et al., Sem. Hematol. 30:16 (1993)). Toxin-targeted delivery technologies, also known as receptor mediated targeting, such as those of Avant Immunotherapeutics, Inc. (Needham, Mass.) may also be used.

[0317] Vaccine compositions often include adjuvants. Many adjuvants contain a substance designed to protect the antigen from rapid catabolism, such as aluminum hydroxide or mineral oil, and a stimulator of immune responses, such as lipid A, Bortadella pertussis or Mycobacterium tuberculosis derived proteins. Certain adjuvants are commercially available as, e.g., Freund's Incomplete Adjuvant and Complete Adjuvant (Difco Laboratories, Detroit, Mich.); Merck Adjuvant 65 (Merck and Company, Inc., Rahway, N.J.); AS-2 (SmithKline Beecham, Philadelphia, Pa.); aluminum salts such as aluminum hydroxide gel (alum) or aluminum phosphate; salts of calcium, iron or zinc; an insoluble suspension of acylated tyrosine; acylated sugars; cationically or anionically derivatized polysaccharides; polyphosphazenes; biodegradable microspheres; monophosphoryl lipid A and quil A. Cytokines, such as GM-CSF, interleukin-2, -7, -12, and other like growth factors, may also be used as adjuvants.

[0318] Vaccines can be administered as nucleic acid compositions wherein DNA or RNA encoding one or more of the polypeptides, or a fragment thereof, is administered to a patient. This approach is described, for instance, in Wolff et. al., Science 247:1465 (1990) as well as U.S. Pat. Nos. 5,580,859; 5,589,466; 5,804,566; 5,739,118; 5,736,524; 5,679,647; WO 98/04720; and in more detail below. Examples of DNA-based delivery technologies include “naked DNA”, facilitated (bupivicaine, polymers, peptide-mediated) delivery, cationic lipid complexes, and particle-mediated (“gene gun”) or pressure-mediated delivery (see, e.g., U.S. Pat. No. 5,922,687).

[0319] For therapeutic or prophylactic immunization purposes, the peptides of the invention can be expressed by viral or bacterial vectors. Examples of expression vectors include attenuated viral hosts, such as vaccinia or fowlpox. This approach involves the use of vaccinia virus, e.g., as a vector to express nucleotide sequences that encode metastatic colorectal cancer polypeptides or polypeptide fragments. Upon introduction into a host, the recombinant vaccinia virus expresses the immunogenic peptide, and thereby elicits an immune response. Vaccinia vectors and methods useful in immunization protocols are described in, e.g., U.S. Pat. No. 4,722,848. Another vector is BCG (Bacille Calmette Guerin). BCG vectors are described in Stover et al., Nature 351:456-460 (1991). A wide variety of other vectors useful for therapeutic administration or immunization e.g., adeno and adeno-associated virus vectors, retroviral vectors, Salmonella typhi vectors, detoxified anthrax toxin vectors, and the like, will be apparent to those skilled in the art from the description herein (see, e.g., Shata et al., Mol Med Today 6:66-71 (2000); Shedlock et al., J. Leukoc Biol 68:793-806 (2000); Hipp et al., In Vivo 14:571-85 (2000)).

[0320] Methods for the use of genes as DNA vaccines are well known, and include placing a metastatic colorectal cancer gene or portion of a metastatic colorectal cancer gene under the control of a regulatable promoter or a tissue-specific promoter for expression in a metastatic colorectal cancer patient. The metastatic colorectal cancer gene used for DNA vaccines can encode full-length metastatic colorectal cancer proteins, but more preferably encodes portions of the metastatic colorectal cancer proteins including peptides derived from the metastatic colorectal cancer protein. In one embodiment, a patient is immunized with a DNA vaccine comprising a plurality of nucleotide sequences derived from a metastatic colorectal cancer gene. For example, metastatic colorectal cancer-associated genes or sequence encoding subfragments of a metastatic colorectal cancer protein are introduced into expression vectors and tested for their immunogenicity in the context of Class I MHC and an ability to generate cytotoxic T cell responses. This procedure provides for production of cytotoxic T cell responses against cells which present antigen, including intracellular epitopes.

[0321] In a preferred embodiment, the DNA vaccines include a gene encoding an adjuvant molecule with the DNA vaccine. Such adjuvant molecules include cytokines that increase the immunogenic response to the metastatic colorectal cancer polypeptide encoded by the DNA vaccine. Additional or alternative adjuvants are available.

[0322] In another preferred embodiment metastatic colorectal cancer genes find use in generating animal models of metastatic colorectal cancer. When the metastatic colorectal cancer gene identified is repressed or diminished in metastatic tissue, gene therapy technology, e.g., wherein antisense RNA directed to the metastatic colorectal cancer gene will also diminish or repress expression of the gene. Animal models of metastatic colorectal cancer find use in screening for modulators of a metastatic colorectal cancer-associated sequence or modulators of metastatic colorectal cancer. Similarly, transgenic animal technology including gene knockout technology, e.g., as a result of homologous recombination with an appropriate gene targeting vector, will result in the absence or increased expression of the metastatic colorectal cancer protein. When desired, tissue-specific expression or knockout of the metastatic colorectal cancer protein may be necessary.

[0323] It is also possible that the metastatic colorectal cancer protein is overexpressed in metastatic colorectal cancer. As such, transgenic animals can be generated that overexpress the metastatic colorectal cancer protein. Depending on the desired expression level, promoters of various strengths can be employed to express the transgene. Also, the number of copies of the integrated transgene can be determined and compared for a determination of the expression level of the transgene. Animals generated by such methods find use as animal models of metastatic colorectal cancer and are additionally useful in screening for modulators to treat metastatic colorectal cancer.

[0324] Kits for Use in Diagnostic and/or Prognostic Applications

[0325] For use in diagnostic, research, and therapeutic applications suggested above, kits are also provided by the invention. In the diagnostic and research applications such kits may include any or all of the following: assay reagents, buffers, metastatic colorectal cancer-specific nucleic acids or antibodies, hybridization probes and/or primers, antisense polynucleotides, ribozymes, dominant negative metastatic colorectal cancer polypeptides or polynucleotides, small molecules inhibitors of metastatic colorectal cancer-associated sequences etc. A therapeutic product may include sterile saline or another pharmaceutically acceptable emulsion and suspension base.

[0326] In addition, the kits may include instructional materials containing directions (i.e., protocols) for the practice of the methods of this invention. While the instructional materials typically comprise written or printed materials they are not limited to such. Any medium capable of storing such instructions and communicating them to an end user is contemplated by this invention. Such media include, but are not limited to electronic storage media (e.g., magnetic discs, tapes, cartridges, chips), optical media (e.g., CD ROM), and the like. Such media may include addresses to internet sites that provide such instructional materials.

[0327] The present invention also provides for kits for screening for modulators of metastatic colorectal cancer-associated sequences. Such kits can be prepared from readily available materials and reagents. For example, such kits can comprise one or more of the following materials: a metastatic colorectal cancer-associated polypeptide or polynucleotide, reaction tubes, and instructions for testing metastatic colorectal cancer-associated activity. Optionally, the kit contains biologically active metastatic colorectal cancer protein. A wide variety of kits and components can be prepared according to the present invention, depending upon the intended user of the kit and the particular needs of the user. Diagnosis would typically involve evaluation of a plurality of genes or products. The genes will be selected based on correlations with important parameters in disease which may be identified in historical or outcome data. TABLE 1 Pkey: Unique Eas probeset identifier nnmber ExAccn: Exemplar Aceession number, Genbank accession nnmber UnigeneID: Unigene number Unigene Title: Unigene gene title Ratio Pkey ExAccn UnigeneID Unigene Title Mets/BS Top 3 expressing cell lines 103989 AA314779 Hs.105484 ESTs; Weakly similar to LITHOSTATHINE 1 15.77 EB_cells, HT29_cells, HMEC 101169 L15533 Hs.423 pancreatitis-associated protein 11.98 HMEC (total RNA), Fibroblasts 2, Fibroblasts 2 101880 M97925 Hs.72887 defensin; alpha 5; Paneth cell-specific 9.24 Fibroblasts 2, MB231_sells, MB-MDA-453 129462 D84239 Hs.111732 IgG Fc binding protein 8.57 EB_cells, OVCAR_cells, HS578T_cells 131676 C20785 Hs.30514 ESTs 7.43 HMEC (total RNA), HMEC, Fibroblasts 2 131861 D11925 Hs.184245 KIAA0929 protein Msx2 interacting nuclea 7.15 HMEC, HMEC (total RNA), Fibroblasts 2 118823 N79237 Hs.50813 ESTs; Weakly similar to long chain fatty 6.72 HMEC, HMEC (total RNA), Lu_AD_H23 101107 L08010 Hs.4158 regenerating islet-derived 1 beta (pancr 6.33 BT474_cells, Fibroblasts 2, MB231_cells 103466 Y00339 Hs.155097 carbonic anhydrase II 6.18 OVCAR_cells, MCF7, 293T_cells 102306 U33317 Hs.711 defensin; alpha 6; Paneth cell-specific 5.67 Fibroblasts 2, HMEC, HT29_cells 126419 AA451775 Hs.129064 H sapiens chromosome 19; cosmid F22162 5.14 HS578T_cells, HMEC (total RNA), HMEC 101198 L21998 Hs.315 mucin 2; intestinal/tracheal 5.1 EB_cells, HT29_cells, MB231_cells 107652 AA010195 Hs.52642 ESTs; Weakly similar to !!!! ALU CLASS F 4.94 HMEC (total RNA), HMEC, EB_cells 128145 AI498467 Hs.166669 ESTs; Weakly similar to sodium bicarbona 4.77 HS578T_cells, HMEC, Lu_SQ_H520 110660 H82117 Hs.28043 ESTs 4.54 HMEC, HS578T_cells, BT474_cells 111669 R19305 Hs.110347 H sapiens mRNA for alpha integrin bindin 4.52 HMEC, HS578T_cells, Caco2 124867 R68971 Hs.188500 ESTs 4.5 HMEC, HMEC (total RNA), HS578T_cells 127352 AA416577 Hs.189105 ESTs 4.41 HMEC, HMEC (total RNA), MB-MDA-435s 130736 T99385 Hs.18646 EST 4.29 HMEC, EB_cells, HMEC (total RNA) 128592 AA470056 Hs.113994 ESTs; Weakly similar to alternatively sp 4.18 HMEC (total RNA), HMEC, Fibroblasts 2 108092 AA045961 Hs.169355 ESTs; Weakly similar to 4.04 HMEC (total RNA), HMEC, Fibroblasts 2 TRANSCRIPTION RE 133373 S72487 Hs.73946 endothellal cell growth factor 1 (platel 4.03 EB_cells, HMEC, HMEC (total RNA) 100572 HG2271 Profilaggrin 4.03 HMEC (total RNA), HMEC, Fibroblasts 2 115775 AA424030 Hs.46627 ESTs 4.02 HMEC, HMEC (total RNA), EB_cells 120811 AA346854 Hs.52788 fragile X mental retardation; autosomal 4.01 HMEC (total RNA), HMEC, Fibroblasts 2 111919 R39926 Hs.21031 ESTs 3.98 EB_cells, HMEC (total RNA), HMEC 117009 H85422 Hs.108556 ESTs 3.97 HMEC (total RNA), HMEC, Fibroblasts 2 101124 L10343 Hs.112341 protease inhibitor 3; skin-derived (SKAL 3.89 PC3_cells, RPWE_2, Caco2 106151 AA424958 Hs.33735 ESTs 3.88 EBsells, HMEC, HMEC (total RNA) 134733 U03644 Hs.89421 CBF1 interacting corepressor 3.88 EB_cells, HMEC, HMEC (total RNA) 131739 AA449749 Hs.31386 ESTs; Highly similar to secreted apoptos 3.87 HS578T_cells, MB-MDA-435s, HT29_cells 116311 AA490469 Hs.48752 ESTs 3.84 HS578T_cells, HMEC, LNCaP_cells 134174 U05259 Hs.79630 CD79A antigen (immunoglobulin-associated 3.83 DU145_cells, Lu_AD_H23, MB231_cells 106753 AA476944 Hs.7331 ESTs 3.82 LNCaP_sells, Lu_SC_H345, DU145_cells 104842 AA039854 Hs.8065 H sapiens mRNA full length insert cDNA c 3.78 HS578T_cells, A549_cells, CALU6_cells 129161 N27334 Hs.181780 ESTs 3.75 HMEC (total RNA), HMEC, BT474_cells 105675 AA284767 Hs.252808 ESTs; Highly similar to pulmonary surfac 3.75 293T_cells, PRSC_con, HT29_cells 100547 HG2149 Mucin (Gb:M57417) 3.75 HMEC (total RNA), HMEC, Fibroblasts 2 116887 H65841 Hs.186550 ESTs 3.73 HS578T_cells, 293T_cells, HMEC 113222 T59670 Hs.10615 ESTs 3.7 HMEC, HS578T_cells, Caco2 118768 N74467 Hs.94304 EST 3.68 HMEC, HS578T_cells, OVCAR_cells 114542 AA055768 Hs.122578 ESTs 3.66 EB_cells, MCF7, LNCaP_cells 101640 M58459 Hs.180911 ribasomal protein S4; Y-linked 3.62 DU145_cells, RPWE_2, A549_cells 107754 AA017462 Hs.187571 ESTs 3.6 HMEC (total RNA), Fibroblasts 2, Fibroblasts 2 104668 AA007312 Hs.183852 ESTs; Weakly similarto polymerase [H.sa 3.58 HMEC (total RNA), HMEC, Fibroblasts 2 135377 C21382 Hs.99768 H sapiens mRNA; cDNA DKFZp564J0323 3.56 HMEC, HMEC (total RNA), EB_cells (from 127083 Z44079 Hs.91608 otoferlin 3.53 HMEC (total RNA), HMEC, Fibroblasts 2 102329 U35407 Hs.158084 peroxisome receptor 1 3.51 HMEC, HMEC (total RNA), EB_cells 117882 N50101 Hs.124724 ESTs; Weakly similar to coded for by C. 3.47 HMEC (total RNA), HMEC, EB_cells 126405 U46278 Hs.122489 ESTs 3.46 LNCaP_cells, MCF7, DU145_cells 131378 AA463886 Hs.203910 small glutamine-rich tetratricopeptide r 3.45 EB_cells, HMEC, HMEC (total RNA) 111418 R01084 Hs.19081 ESTs 3.43 HS578_Tcells, EB_cells, Lu_AD_H23 135398 AA194075 Hs.99908 nuclear receptor coactivator 4 3.4 HS578_Tcells, EB_cells, HMEC 108710 AA121960 zm24g9.sl Stratagene pancreas (#93728) H 3.4 EB_cells, HMEC, HMEC (total RNA) mRNA seq 105437 AA252191 Hs.25199 ESTs; Highly similar to match to ESTsAA 3.38 EB_cells, LNCaP_cells, RPWE_2 103448 X99133 Hs.204238 lipocalin 2 (oncogene 24p3) 3.38 PC3_cells, EB_cells, HT29_sells 130436 M84526 Hs.155597 D component of complement (adipsin) 3.37 PRSC_con, EB_cells, Lu_AD_H23 112309 R55021 yj76d5.s1 Soares breast 2NbHBst H sapien 3.36 EB_cells, HMEC, HMEC (total RNA) 103211 X73079 Hs.205126 polymeric immunoglobulin receptor 3.35 MB231_cells, HT29_cells, Lu_SC_H69 109012 AA156576 Hs.191466 ESTs 3.21 EB_cells, HMEC, HMEC (total RNA) 129989 AF005887 Hs.247433 activating transcription factor 6 3.19 HMEC (total RNA), HMEC, Lu_AD_H23 113466 T86945 Hs.16304 ESTs 3.18 HMEC, MB231_cells, Caco2 103029 X54489 Hs.789 GRO1 oncogene (melanoma growth stimulati 3.16 Lu_LC_H460, PC3_cells, Fibroblasts 2 109374 AA218727 Hs.210785 ESTs; Highly similar to lbd1 [H.sapiens] 3.13 Caco2, A549_cells, MB231_cells 131403 R55750 Hs.26455 ESTs 3.13 HS578T_cells, HMEC, MB231_cells 113420 T83964 Hs.15400 ESTs 3.11 HMEC (total RNA), HMEC, EB_cells 112532 R69824 Hs.28313 ESTs 3.11 HMEC, HMEC (total RNA), EB_cells 117905 N50782 Hs.231713 EST 3.11 HMEC, HS578T_cells, Caco2 125349 T87826 Hs.164480 ESTs 3.1 HS578T_cells, EB_cells, MB-MDA-435s 107072 AA609113 Hs.177533 H sapiens mRNA; cDNA DKFZp586N0318 3.1 Lu_SC_H69, MB-MDA-453, MB231_cells (from 118389 N64583 Hs.182365 ESTs 3.05 HMEC, HMEC, LNCaP_cells 117653 N38970 Hs.194214 ESTs 3.04 HMEC, HMEC (total RNA), Fibroblasts 2 101082 L05072 Hs.80645 interferon regulatory factor 1 3.04 EB_cells, PRSC_con, DU145_cells 126105 H75323 Hs.167614 ESTs 3.03 HS578T_cells, HMEC (total RNA), HMEC 120006 W90108 Hs.10848 KIAA0187 gene product 3.03 HMEC, HMEC (total RNA), EB_cells 127191 AA297581 EST113160 Gall bladder I H sapiens cDNA 3.02 HMEC, Lu_AD_H23, Lu_SQ_H520 106899 AA490107 Hs.21753 JM5 protein 3.02 EB_cells, HMEC (total RNA), HMEC 112784 R96306 Hs.191290 ESTs 3.02 EB_cells, HMEC, Lu_AD_358 113613 T93337 Hs.17167 ESTs; Highly similar to LRR FLI-l intera 3.02 HMEC (total RNA), EB_cells, HMEC 107631 AA007230 Hs.95026 ESTs 3.02 Lu_SC_H345, HS578T_cells, Lu_LC_H460 101923 S75256 HNL = neutrophil lipocalin [human, ovarian 3.01 PC3_cells, EB_cells, HT29_cells 100695 HG315T Beta-1-Glycoprotein 11, Pregnancy-Specif 3.01 Fibroblasts 2, Lu_AD_H23, MB-MDA-435s 102523 U53445 Hs.15432 downregulated in ovarian cancer 1 2.98 PRSC_con, Fibroblasts 2, HMEC 121588 AA416615 Hs.98242 ESTs 2.94 HMEC, HS578T_cells, BT474_cells 103714 AA047055 Hs.192943 ESTs 2.94 HS578T_cells, EB_cells, HMEC 104916 AA056588 Hs.16542 ESTs 2.93 HMEC (total RNA), Fibroblasts 2, HMEC 109928 H05961 Hs.26331 ESTs 2.92 HMEC, MB231_cells, HS578T_cells 104586 R78309 Hs.20787 ESTs 2.92 Caco2, Lu_AD_358, Lu_AD_358 101236 L29433 Hs.47913 coagulation factor X 2.91 HMEC, HS578T_cells, Caco2 134749 L10955 Hs.89485 carbonic anhydrase IV 2.9 BT474_cells, MCF7, HMEC (total RNA) 124703 R07294 Hs.109108 solute carrier family 22 (organic cation 2.9 HMEC, HMEC (total RNA), MB-MDA-435s 114108 Z38431 Hs.27038 ESTs; Moderately similar to X-linkod ret 2.89 HMEC, HMEC (total RNA), EB_cells 107857 AA024687 Hs.61208 ESTs 2.88 HS578T_cells, MB231_cells, HMEC 111586 R10759 Hs.15177 ESTs 2.88 HS578T_cells, Lu_LC_H460, PRSC_con 127553 AA282433 H sapiens p60 katanin mRNA; complete cds 2.87 EB_cells, MB-MDA-435s, RPWE_2 129881 AA458952 Hs.197728 ESTs; Weakly similar to ZINC FINGER PROT 2.86 EB_cells, PC3_cells, HMEC 116852 H65459 Hs.38323 ESTs 2.85 HMEC, Caco2, HS578T_cells 133468 X03068 Hs.73931 major histocompatibility complex; class 2.82 MB-MDA-435s, BT474_cells, HT29_cells 130998 C00810 Hs.21970 guanine nucleotide binding protein (G pr 2.82 LNCaP_cells, Lu_SC_H345, E8_cells 124075 H05741 Hs.101643 ESTs 2.82 HMEC, HS578T_cells, HT29_cells 128108 AI247422 Hs.129966 ESTs 2.82 HS578T_cells, Lu_LC_H1460, Lu_SC_H69 128096 R15413 Hs.164919 ESTs; Highly similarto PROTEIN KINASE C 2.8 MB231_cells, Lu_AD_H23, RPWE_2 126619 Z28861 HSBA7E032 STRATAGENE Human skeletal musc 2.77 HMEC, Lu_AD_H23, HMEC (total RNA) cDNA clone A7E03, mRNA seq. 114418 AA011383 Hs.177313 ESTs 2.77 HS578T_cells, EB_cells, MCF7 120383 AA228030 Hs.120234 ESTs 2.77 EB_cells, Fibroblasts 2, HMEC (total RNA) 126535 H73017 Hs.250723 ESTs; Weakly similar to atrophin-1 relat 2.76 Fibroblasts 2, PRSC_con, DU145_cells 119347 T64349 yc10d0B.s1 Stratagene lung (#937210) H s 2.76 EB_cells, Lu_AD_H23, Lu_SC_H69 126219 N36368 Hs.141438 ESTs; Moderately similar to similar to C 2.76 Lu_AD_H23, HMEC (total RNA), MB-MDA-435s 125426 R43963 Hs.169355 ESTs; Weakly similar to TRANSCRIPTION RE 2.75 HMEC, HMEC (total RNA), Lu_SC_H69 103005 X52008 Hs.2700 glycine receptor; alpha 2 2.74 HS578T_cells, HMEC, MB-MDA-453 109170 AA180352 Hs.191472 ESTs 2.74 Fibroblasts 2, HMEC (total RNA), MB-MDA-435s 101125 L10373 Hs.82749 transmembrane 4 superfamily member 2 2.73 Lu_LC_H460, 293T_cells, EB_cells 130656 Z20481 Hs.17411 KIAA0699 protein 2.73 HMEC (total RNA), HMEC, Fibroblasts 2 122933 AA476728 Hs.107537 ESTs 2.72 HMEC, EB_cells, HMEC (total RNA) 126033 AA055978 Hs.3807 ESTs; Weakly similar to PHOSPHOLEMMAN PR 2.71 Lu_SC_H345, Lu_SC_H69, 293T_cells 111644 R16539 Hs.223649 EST; Moderately similar to Cd-7 Metallo 2.71 EB_cells, HMEC, HMEC (total RNA) 133719 AA033790 Hs.75736 apolipoprotein D 2.71 Caco2, Fibroblasts 2, MB-MDA-435s 127555 AA582324 Hs.192857 ESTs 2.7 HMEC, HS578T_cells, HMEC (total RNA) 113321 T70580 Hs.13759 ESTs 2.69 HMEC (total RNA), Fibroblasts 2, PRSC_con 109326 AA210719 Hs.86414 ESTs 2.68 MB-MDA-435s, HS578T_cells, Lu_SC_H69 135003 H42527 Hs.92832 ESTs 2.68 HS578T_cells, EB_cells, PRSC_con 103650 Z70220 H.sapiens mRNA for 5′UTR for unknown pro 2.68 HMEC, HS578T_cells, PRSC_con 111507 R07728 Hs.191218 ESTs 2.67 HMEC (total RNA), HMEC, EB_cells 117084 H93081 Hs.41829 ESTs 2.67 HS578T_cells, HMEC, MB231_cells 103975 AA306264 Hs.176403 ESTs; Moderately similar to !!!! ALU SUB 2.67 DU145_cells, HS578T_cells, MB-MDA-435s 132850 R89741 Hs.58215 ESTs; Moderately similar to rhotekin [M. 2.66 HS578T_cells, EB_cells, 293T_cells 121599 AA416770 Hs.98255 EST 2.61 HMEC (total RNA), HMEC, EB_cells 124230 H63111 Hs.6655 ESTs 2.6 HMEC (total RNA), HMEC, Fibroblasts 2 114174 Z39055 Hs.27264 ESTs; Moderately similar to !!!! ALU SUB 2.58 Caco2, MB-MDA-453, A549_cells 128469 T23724 Hs.258677 EST 2.57 Lu_LC_H460, Lu_SC_H69, MB-MDA-435s 117399 N26480 Hs.43805 lipoma HMGIC fusion partner-like 3 2.57 HMEC, HMEC (total RNA), EB_cells 129279 AA460551 Hs.184860 ESTs; Weakly similar to EG:87B1.6 [D.mel 2.57 HS578T_cells, EB_cells, HT29_cells 119817 W74257 Hs.159690 ESTs 2.57 HMEC, HMEC (total RNA), Lu_SC_H69 114445 AA019594 Hs.250493 ESTs; Weakly similar to KIAA0390 [H.sapi 2.56 HMEC, HT29_cells, Lu_LC_H460 120651 AA287286 Hs.99657 ESTs 2.55 HMEC, HMEC (total RNA), Fibroblasts 2 105707 AA291012 Hs.37617 ESTs; Weakly similar to KIAA0727 protein 2.55 HMEC (total RNA), EB_cells, BT474_cells 128483 T58588 Hs.5148 FLN29 gene product 2.54 HMEC, HS578T_cells, MB231_cells 125890 AA448739 Hs.116708 ESTs; Weakly similar to HYPOTHETICAL PRO 2.54 HMEC (total RNA), HMEC, OVCAR_cells 134764 M74715 Hs.89560 iduronidase; alpha-L- 2.54 BT474_cells, PRSC_con, HT29_cells 113404 T82323 Hs.70337 immunoglobulin superfamily; member 4 2.54 Caco2, HS578T_cells, HMEC 129128 AA423854 Hs.108812 ESTs 2.54 BT474_cells, MB-MDA-435s, HMEC 101428 M19684 Hs.184929 protease inhibitor 1 (alpha-1-antitrypsi 2.54 HMEC, HT29_cells, HMEC (total RNA) 103206 X72755 Hs.77367 monokine induced by gamma interferon 2.53 Fibroblasts 2, MB231_cells, HMEC (total RNA) 132273 AA489716 Hs.43658 DKFZP586L151 protein 2.53 EB_cells, HMEC, HMEC (total RNA) 108392 AA075124 zm86a1.s1 Stratagene ovarian cancer (#93 2.52 HMEC (total RNA), HMEC, HS578T_cells IMAGE:544776 3′, mRNA seq 119508 W37895 Hs.45519 ESTs 2.52 Lu_SC_H69, CALU6_cells, 293T_cells 109828 F13763 Hs.19827 ESTs 2.52 PRSC_log, PRSC_con, HS578T_cells 135096 N89775 Hs.132390 zinc finger protein 36 (KOX 18) 2.51 HMEC, HS578T_cells, HT29_cells 130860 U66061 Hs.241395 protease; seine; 1 (trypsin 1) 2.51 OVCAR_cells, MB231_cells, PC3_cells 105725 AA292228 Hs.199791 STAT induced STAT inhibitor 3 2.51 HS578T_cells, HT29_cells, HMEC 110427 H48579 Hs.36275 EST 2.51 HS578T_sells, Caco2, Lu_LC_H460 123762 AA610013 Hs.244553 EST 2.51 HMEC (total RNA), HMEC, Fibroblasts 2 126406 AA034096 zi06f05.r1 Soares_fetal_liver_spleen_1NF 2.5 Lu_AD_H23, HS578T_cells, Lu_AD_358 IMAGE:430017 5′, mRNA seq. 129751 AA346065 Hs.111286 KIAA0714 protein 2.5 HMEC, HS578T_cells, Fibroblasts 2 121704 AA418743 Hs.98306 ESTs 2.5 EB_cells, HMEC (total RNA), HMEC 112595 R77783 Hs.22404 protease; serine; 12 (neurotrypsin; moto 2.5 Fibroblasts 2, EB_cells, PRSC_son 108499 AA083103 zn1b12.s1 Stratagene hNT neuron (#937233 2.5 LNCaP_cells, MB-MDA-453, HMEC IMAGE:5477 3′, mRNA seq 131968 AA151333 Hs.36029 ESTs; Highly similar to basic helix-loop 2.5 Fibroblasts 2, A549_cells, 293T_cells 112665 R85661 Hs.221447 ESTs 2.48 Lu_AD_H23, HMEC, Lu_LC_H460 115764 AA421562 Hs.91011 anterior gradient 2 (Xenepus laevis) hom 2.48 EB_cells, Caco2, MCF7 105959 AA405540 Hs.7001 ESTs 2.48 OVCAR_cells, BT474_cells, Caco2 125804 R79519 Hs.16899 ESTs 2.48 HMEC (total RNA), EB_cells, HMEC 110102 H16681 Hs.180950 guanine nucleotide binding protein (G pr 2.46 HS578T_cells, HMEC, OVCAR_cells 104680 AA009809 Hs.37599 ESTs 2.46 HMEC, HS578T_cells, Caco2 132339 D80030 Hs.45127 chondroitin sulfate proteoglycan 5 (neur 2.45 OVCAR_cells, 293T_cells, HMEC (total RNA) 121712 AA419116 Hs.193663 ESTs; Weakly similar to !!!! ALU SUBFAMI 2.45 Lu_SQ_H520, Lu_AD_H23 Lu_SC_H69 129226 M96843 Hs.180919 inhibitor of DNA binding 2; dominant neg 2.44 MB-MDA-453, 293T_cells, Caco2 128731 AF005271 Hs.104555 neuropeptide FF-amide peptide precursor 2.43 HMEC, HMEC (total RNA), EB_cells 106670 AA461174 Hs.5943 ESTs 2.43 EB_cells, HS578T_cells, Lu_SC_H69 119306 T26914 Hs.132785 EAP30 subunit of ELL complex 2.43 EB_cells, HMEC (total RNA), HMEC 133507 X74295 Hs.74369 integrin; alpha 7 2.42 Fibroblasts 2, Caco2, EB_cells 125713 AA367905 Hs.77356 transferrin receptor (p90; CD71) 2.41 HS578T_cells, Fibroblasts 2, Lu_AD_H23 107438 W27841 Hs.17118 ESTs; Weakly similar to B0025.2 ]C.elega 2.41 HMEC, HS578T_cells, MB231_cells 101784 M83186 Hs.114346 cytochrome c oxidase subunit VIIa polype 2.41 Fibroblasts 2, PRSC_con, PRSC_log 134578 AA194724 Hs.182418 endonuclease G 2.4 EB_cells, HMEC, Lu_AD_H23 125105 T95642 Hs.189759 ESTs 2.4 EB_cells, A549_cells, HS578T_cells 127067 AA380418 Hs.88012 SHP2 interacling transmembrane adaptor 2.4 HMEC, HMEC (total RNA), EB_cells 113118 T47906 Hs.220512 ESTs 2.39 MB-MDA-435s, HS578T_cells, HMEC 104791 AA029046 Hs.30377 ESTs; Moderately similar to dAMP inducib 2.39 LNCaP_cells, OVCAR_cells, PC3_cells 115833 AA428269 Hs.125035 ESTs 2.38 Caco2, LNCaP_cells, CALU6_cells 132223 R77451 Hs.4245 ESTs; Weakly similar to similar to S. ce 2.38 HMEC, HMEC (total RNA), EB_cells 115836 AA428863 Hs.89388 ESTs 2.38 HS578T_cells, HMEC, PRSC_con 101891 S45630 Hs.1940 crystallin; alpha B 2.38 HS578T_cells, OVCAR_cells, Lu_LC_H460 132894 D82422 Hs.5944 ESTs 2.37 Caco2, MB-MDA-453, HT29_cells 106939 AA496048 Hs.26570 ESTs 2.35 LNCaP_cells, 293T_cells, EB_cells 131104 W27770 Hs.258721 ESTs 2.35 HMEC (total RNA), HMEC, HT29_cells 122355 AA443789 Hs.189324 ESTs 2.34 HMEC (total RNA), HMEC, EB_cells 119343 T62873 yc3d2.s1 Stratagene lung (#93721) H sapi 2.34 HS578T_cells, Lu_SC_H69, HT29_cells to contains Alu repetitive element;, mR 115442 AA284722 Hs.89121 H sapiens mRNA; chromosome 1 specific tr 2.33 Lu_AD_H23, HMEC (total RNA), BT474_cells 134286 T69384 Hs.68398 period (Drosophila) homolog 1 2.33 HMEC, HMEC (total RNA), MB231_cells 125465 AI375276 Hs.158732 ESTs 2.33 HMEC (total RNA), EB_cells, HMEC 127449 AI421866 Hs.75722 ribophorin II 2.33 Lu_AD_H23, HMEC (total RNA), HMEC 110225 H23927 Hs.222381 ESTs 2.33 HS578T_cells, HMEC, Lu_LC_H460 119930 W86471 Hs.151624 hypocretin (orexin) receptor 2 2.32 HMEC, HMEC (total RNA), EB_cells 125958 AI073357 Hs.12311 H sapiens clone 23570 mRNA seq 2.32 MB231_cells, HMEC (total RNA), HMEC 119746 W70279 Hs.221189 ESTs; Weakly similar to 15-HYDROXYPROSTA 2.32 HMEC, HS578T_cells, MB231_cells 108874 AA134112 Hs.107187 H sapiens DNA seq from cosmid ICK072IQ o 2.32 Caco2, PRSC_con, LNCaP_cells L12 LIKE protein in an intron of the HS 127368 AA434362 Hs.193326 ESTs 2.32 HMEC (total RNA), HS578T_cells, HMEC 120437 AA243427 Hs.104311 ESTs 2.32 HMEC (total RNA), HMEC, MB-MDA-435s 119867 W80852 Hs.250696 KDEL (Lys-Asp-Glu-Leu) endoplasmic retic 2.32 Fibroblasts 2, HS578T_cells, MB-MDA-435s 131205 J02947 Hs.2420 superoxide dismutase 3; extracellular 2.32 PRSC_con, EB_cells, Lu_AD_358 133710 X76057 Hs.75694 mannose phosphate isomerase 2.31 293T_cells, LNCaP_cells, RPWE_2 104834 AA039331 Hs.16323 ESTs; Weakly similar to GAGE-7 [H.sapien 2.31 Caco2, HS578T_cells, HMEC 113186 T56048 Hs.189674 ESTs 2.31 HMEC, Fibroblasts 2, HMEC (total RNA) 113462 T86826 Hs.142528 ESTs 2.31 PC3_cells, HS578T_cells, HMEC 104743 AA0211157 Hs.33619 ESTs 2.3 HMEC (total RNA), HMEC, OVCAR_cells 129687 Y00097 Hs.118796 annexin A6 2.3 PRSC_log, PRSC_con, HS578T_cells 111573 R10305 Hs.185683 ESTs 2.3 HMEC, HMEC (total RNA), EB_cells 117523 N32626 Hs.145532 ESTs; Weakly similar to Gag polyprotein 2.29 EB_cells, Fibroblasts 2, HS578T_cells 115540 AA349954 Hs.56281 ESTs; Weakly similar to ASB-1 protein [H 2.29 Fibroblasts 2, BT474_cells, MB231_cells 101622 M55621 Hs.151513 mannosyl (alpha-1;3-)-glycoprotein beta- 2.29 PRSC_con, RPWE_2, PRSC_log 103535 Y13620 Hs.122607 B-cell CLL/lymphoma 9 2.28 Lu_SC_H69, Lu_AD_358, Lu_AD_H23 127482 AI337294 Hs.155014 ESTs 2.28 HS578T_cells, 293T_cells, CALU6_cells 104297 D31111 Hs.106005 ESTs; Highly similar to NY-REN-50 antige 2.27 EB_cells, DU145_cells, HT29_cells 112318 R55470 Hs.11067 ESTs 2.27 MB-MDA-453, LNCaP_cells, OVCAR_cells 101877 M97496 Hs.778 guanylate cyclase activator 1B (retina) 2.27 HT29_cells, BT474_cells, Caco2 100760 HG3576 Major Histocompatibility Complex, Class 2.26 MB-MDA-435s, MB231_cells, BT474_cells 102362 U39412 Hs.75932 N-ethylmaleimide-sensitive factor attach 2.26 LNCaP_cells, MB-MDA-453, Caco2 106142 AA424590 Hs.239631 Golgi transport complex protein (90 kDa) 2.26 HMEC, HS578T_cells, Caco2 101461 M22430 Hs.76422 phospholipase A2; group IIA (platelets; 2.26 LNCaP_cells, BT474_cells, Caco2 119336 T55340 Hs.208238 ESTs 2.26 HS578T_cells, EB_cells, HMEC 127619 AA627122 Hs.163787 ESTS 2.25 Lu_SQ_H520, Lu_LC_H460, Lu_SC_H69 104113 AA427510 Hs.181202 ESTs; Weakly similar to Wiscott-Aldrich 2.25 MB-MDA-435s, Fibroblasts 2, HMEC (total RNA) 131219 C00476 Hs.24395 small inducible cytokine subfamily B (Cy 2.25 Lu_SQ_H520, BT474_cells, Fibroblasts 2 118915 N91481 Hs.54713 ESTs 2.25 HMEC (total RNA), HMEC, MCF7 127556 AA679831 Hs.190228 ESTs 2.24 HS578T_cells, EB_cells, HMEC 128700 U59286 Hs.103982 small inducible cytokine subfamily B (Cy 2.24 HMEC, HS578T_cells, Fibroblasts 2 113674 T96374 Hs.5753 Inositol(myo)-1(or 4)-monophosphatase 2 2.24 A549_cells, DU145_cells, Lu_AD_358 133085 M73720 Hs.646 carboxypeptidase A3 (mast cell) 2.24 HS578T_cells, Fibroblasts 2, HT29_cells 106017 AA411882 Hs.26268 ESTs 2.24 MB-MDA-453, OVCAR_cells, 293T_cells 100582 HG2348 Peptide Yy 2.24 HMEC, HS578T_cells, HMEC (total RNA) 134811 N66357 Hs.89761 ATP synthase; H+ transporting; mitochond 2.23 Lu_SQ_H520, LNCaP_cells, Lu_AD_H23 102543 U57627 Hs.234776 oculocerebrorenal syndrome of Lowe 2.23 293T_cells, EB_cells, LNCaP_cells 127357 AA452788 zx39g11.r1 Soares_total_fetus_Nb2HF8_9w 2.23 HS578T_cells, RPWE_2, HMEC (total RNA) IMAGE:788900 5′, mRNA seq. 135288 AA402930 Hs.97876 ESTs 2.23 HS578T_cells, 293T_cells, OVCAR_cells 105581 AA278850 Hs.28891 ESTs; Weakly similar to !!!! ALU SUBFAMI 2.23 BT474_cells, BT474_cells, MB231_cells 103812 AA137107 Hs.124094 ESTs; Weakly similarto NFAT1-A [M.muscu 2.23 Lu_SC_H345, Lu_AD_H23, PRSC_con 117016 H87171 Hs.52170 ESTs 2.22 Fibroblasts 2, Lu_LC_H460, HMEC (total RNA) 114607 AA079342 Hs.129057 breast carcinoma amplified seq 1 2.22 BT474_cells, HT29_cells, HT29_cells 134000 U29091 Hs.7833 selenium binding protein 1 2.22 LNCaP_cells, MB-MDA-453, BT474_cells 111069 N58461 Hs.22036 ESTs 2.22 HMEC, Lu_SC_H345, HS578T_cells 129048 L27670 Hs.108287 intercellular adhesion molecule 4; Lands 2.21 Lu_AD_H23, HS578T_cells, Lu_SQ_H520 124995 T52700 Hs.110044 ESTs 2.2 Caco2, MB-MDA-453, HT29_cehls 116678 F05063 Hs.251736 ESTs 2.2 HS578T_cells, BT474_cells, 293T_cells 118222 N62263 Hs.48501 EST 2.2 HS578T_cells, BT474_cells, MB231_cells 127888 AI149662 Hs.143590 ESTs 2.19 BT474_cells, CALU6_cells, MB231_cells 113790 W33178 Hs.26912 ESTs 2.19 HMEC, HMEC (total RNA), Fibroblasts 2 100097 AF002224 H sapiens Angelman Syndrome Gene, E6-AP 2.19 HS578T_cells, CALU6_cells, 293T_cells from promoter P1, 5′UTR 109151 AA176800 Hs.73452 ESTs 2.19 CALU6_cells, Lu_AD_H23, Lu_SC_H69 135368 AA086057 Hs.9964 ribosomal protein; mitochondrial; S12 2.19 OVCAR_cells, A549_cells, Lu_AD_H23 109016 AA156936 Hs.58069 ESTs; Highly similar to type II cAMP-dep 2.19 HS578T_cells, BT474_cells, A549_cells 124300 H92575 Hs.105959 ESTs; Weakly similar to !!!! ALU SUBFAMI 2.18 Lu_AD_358, Lu_SC_H69, Lu_SC_H345 123450 AA598913 Hs.111207 ESTs 2.18 HMEC (total RNA), HMEC, MB-MDA-435s 117435 N27628 yw50b08.s1 Weizmann Olfactory Epithelium 2.18 LNCaP_cells, DU145_cells, Lu_SQ_H520 119860 W80709 Hs.58485 ESTs 2.18 HS578T_cells, MB231_cells, Caco2 123833 AA620717 Hs.112889 ESTs 2.18 Lu_AD_H23, Lu_SQ_H520, Lu_AD_358 107936 AA029446 Hs.53115 ESTs 2.17 Caco2, 293T_cells, 293T_cells 119380 T83659 Hs.184407 ESTs 2.16 Lu_AD_H23, Lu_AD_358, PRSC_con 114066 Z38152 Hs.26920 ESTs 2.15 HMEC (total RNA), HMEC, EB_cells 128748 T59001 Hs.10475 ESTs 2.15 HMEC, HT29_cells, MB231_cells 130414 M21121 Hs.241392 small inducible cytokine A5 (RANTES) 2.15 HS578T_cells, PC3_cells, A549_cells 123490 AA599723 TAP binding protein (tapasin) 2.15 HS578T_cells, EB_cells, Lu_SC_H69 112588 R77302 Hs.20226 ESTs 2.14 HMEC (total RNA), HMEC, Fibroblasts 2 110548 H58715 Hs.14706 ESTs 2.14 HMEC, HMEC (total RNA), HT29_cells 101581 M34996 Hs.198253 major histocompatibility complex; class 2.14 MB-MDA-435s, HMEC, HMEC 115248 AA278887 Hs.194530 ESTs; Weakly similarto unknown [H.sapie 2.14 HT29_cells, BT474_cells CALU6_cells 105619 AA280810 Hs.24003 ESTs; Moderately similar to LEYDIG CELL 2.14 Lu_SQ_H520, MB-MDA-435s, LNCaP_cells 128058 AI126617 Hs.132449 ESTs 2.14 HS578T_cells, EB_cells, HMEC (total RNA) 134573 AA442125 Hs.171873 ESTs; Weakly similar to PUTATIVE STEROID 2.14 EB_cells, MB231_cells, Caco2 134863 AA353903 Hs.183373 ATX1 (antioxidant protein 1; yeast) homo 2.14 Lu_SC_H345, HT29_cells, BT474_cells 128811 H17317 Hs.169100 ESTs; Weakly similar to HPBRII-7 protein 2.13 Caco2, Lu_SC_H345, EB_cells 112368 R59371 Hs.26653 EST 2.13 HMEC, HMEC (total RNA), Lu_SQ_H520 108395 AA075144 zm86f6.s1 Stratagene ovarian cancer (#93 2.13 HMEC (total RNA), HMEC, OVCAR_cells gb:X1664 TRANSLATIONALLY CONTROLLED TUM 129611 D45680 Hs.11614 ESTs 2.13 HMEC, HS578T_cells, Caco2 101253 L34355 Hs.99931 sarcoglycan; alpha (50 kD dystrophin-asso 2.12 HS578T_cells, OVCAR_cells, CALU6_cells 126701 AA515212 Hs.202590 ESTs; Weakly similar to mucin glycoprote 2.12 EB_cells, Lu_AD_H23, Lu_AD_H23 111628 R15825 Hs.4014 KIAA0940 protein; Huntingtin interacting 2.12 A549_cells, BT474_cells, MB-MDA-435s 108675 AA115240 Hs.61816 ESTs 2.12 Lu_AD_H23, MB-MDA-453, PRSC_con 127131 Z44658 Hs.105460 DKFZP564O0823 protein 2.12 EB_cells, Lu_SC_H69, Lu_SC_H69 109590 F02465 Hs.27281 ESTs 2.12 HMEC, HS578T_cells, HMEC (total RNA) 116539 D12124 Hs.242890 EST 2.12 Lu_AD_H23, Caco2, BT474_cells 112117 R45402 Hs.23789 ESTs 2.12 EB_cells, Lu_AD_H23, Lu_SQ_H520 126367 AA477929 Hs.25584 ESTs 2.12 Lu_SC_H69, Lu_AD_H23, Lu_AD_358 135252 U62966 Hs.97207 solute carrier family 28 (sodium-coupled 2.11 MB-MDA-435s, 293T_cells, CALU6_cells 117565 N34301 Hs.248426 EST 2.11 HMEC, HS578T_cells, MB231_cells 129430 AA258842 Hs.197877 H sapiens clone 23777 putative transmemb 2.11 HS578T_cells, Lu_AD_358, MB-MDA-435s 120256 AA169801 sema domain; immunoglobulin domain (lg); 2.11 HMEC, HMEC (total RNA), EB_cells 134169 D20342 Hs.178137 transducer of ERBB2; 1 (TOB1) 2.11 HMEC (total RNA), 293T_cells, OVCAR_cells 130397 AA487452 Hs.155344 DNA fragmentation factor; 45 kD; alpha s 2.11 293T_cells, Caco2, Lu_AD_H23 132859 D20925 Hs.5842 ESTs 2.11 HMEC (total RNA), Fibroblasts 2, HMEC 117633 N36404 Hs.44807 ESTs 2.11 HMEC, Caco2, HS578T_cells 125003 T59442 Hs.100445 ESTs 2.11 MB-MDA-435s, HMEC (total RNA), HT29_cells 125329 AA825437 Hs.58875 ESTs 2.11 HS578T_cells, PRSC_con, PRSC_log 114065 Z38149 Hs.134015 uronyl 2-sulfotransferase 2.11 MB-MDA-435s, 293T_cells, PRSC_con 120718 AA292747 Hs.97296 ESTs 2.11 HT29_cells, Lu_AD_H23, Lu_SC_H69 133869 T49444 Hs.77031 Sp2 transcription factor 2.1 Lu_LC_H460, Lu_AD_358, RPWE_2 135351 AA430179 Hs.9933 putative Ac-like transposon 2.1 HS578T_cells, EB_cells, HMEC 110973 N51529 Hs.118047 ESTs 2.09 EB_cells, HS578T_cells, MCF7 131879 AA017161 Hs.33792 ESTs 2.09 HMEC (total RNA), MB231_cells, BT474_cells 116656 F03935 Hs.241640 EST 2.09 HS578T_cells, Lu_LC_H460, Lu_SC_H69 120311 AA194074 Hs.193401 ESTs 2.09 OVCAR_cells, HMEC (total RNA), HMEC 108024 AA040433 Hs.61898 DKFZP586N2124 protein 2.09 HMEC (total RNA), BT474_cells, HT29_cells 105871 AA399633 Hs.24872 ESTs 2.09 Fibroblasts 2, A549_cells, HS578T_cells 120206 Z40805 Hs.91668 ESTs 2.09 BT474_cells, MB-MDA-453, EB_cells 112333 R56222 Hs.26514 ESTs 2.09 Lu_AD_H23, Fibroblasts 2, Lu_LC_H460 116746 H04811 Hs.79027 ESTs 2.08 MB-MDA-435s, HMEC (total RNA), Lu_SC_H345 121529 AA412257 Hs.98121 ESTs 2.08 HMEC, HMEC (total RNA), HS578T_cells 105592 AA279337 Hs.180549 ESTs; Highly similar to R26660_1; partia 2.08 LNCaP_cells, PRSC_log, PRSC_log 108582 AA088231 Hs.91732 ESTs 2.08 HS578T_cells, Lu_SC_H345, Lu_SC_H69 123197 AA489250 Hs.59403 serine palmitoyltransferase; subunit II 2.08 EB_cells, Lu_SC_H69, Lu_SC_H345 134965 J05480 Hs.92 protein phosphatase 3 (formerly 2B); cat 2.08 LNCaP_cells, MB-MDA-435s, HMEC 123856 AA620814 Hs.144959 ESTs 2.08 HS578T_cells, BT474_cells, BT474_cells 132058 AA251737 Hs.172818 Apg12 (autophagy 12; S. cerevisiae)-like 2.07 HS578T_cells, MCF7, HMEC 126476 R94666 Hs.195155 ESTs; Weakly similar to transporter prot 2.07 PRSC_log, Lu_LC_H460, RPWE_2 106087 AA418740 Hs.21111 ESTs 2.07 OVCAR_cells, A549_cells, Lu_AD_H23 103802 AA122003 Hs.62954 ferritin; heavy polypeptide 1 2.07 HMEC, HMEC (total RNA), HS578T_cells 125633 AA908225 Hs.126641 ESTs 2.07 EB_cells, Flbroblasts 2, Lu_SC_H69 112817 R98491 Hs.14584 ESTs 2.07 HMEC, HMEC (total RNA), Fibroblasts 2 111050 N56984 Hs.74335 heat shock 90 kD protein 1; beta 2.07 LNCaP_cells, DU145_cells, 293T_cells 133072 AA425294 Hs.64322 ESTs; Weakly similar to Closely related 2.07 LNCaP_cells, MB-MDA-453, Caco2 118270 N62868 Hs.48653 ESTs 2.07 HMEC (total RNA), HMEC, EB_cells 105035 AA128406 Hs.8859 ESTs 2.07 LNCaP_cells, PC3_cells, EB_cells 102337 U36922 Human fork head domain protein (FKHR) mR 2.07 293T_cells, HMEC, HT29_cells 109687 F09380 Hs.182859 lifeguard 2.06 BT474_cells, BT474_cells, Lu_AD_H23 109802 F10789 Hs.12439 ESTs 2.06 EB_cells, EB_cells, Caco2 128103 AA905960 Hs.48516 ESTs 2.06 HT29_cells, HMEC (total RNA), HMEC 128278 AI018343 Hs.131275 ESTs 2.06 PRSC_con, Lu_SC_H345, HS578T_cells 131873 H39997 Hs.33716 ESTs 2.08 HMEC (total RNA), HMEC, EB_cells 122683 AA455528 Hs.96772 ESTs 2.05 LNCaP_cells, Lu_AD_H23, HS578T_cells 128066 AA884838 Hs.189171 ESTs 2.05 HMEC, HUEC (total RNA), Fibroblasts 2 131451 N28028 Hs.26968 H sapiens mRNA from chromosome 5q21-22; 2.05 MB-MDA-435s, Lu_LC_H460, Lu_SQ_H520 120887 AA365644 Hs.97043 ESTs 2.05 HS578T_cells, PRSC_con, HMEC 103966 AA303166 Hs.127270 ESTs 2.05 HMEC (total RNA), LNCaP_cells, PC3_cells 105861 AA399260 Hs.28454 ESTs 2.05 Fibroblasts 2, HMEC (total RNA), EB_cells 104627 AA001976 Hs.19603 ESTs 2.05 HS578T_cells, HMEC, BT474_cells 108794 AA129468 Hs.203392 ESTs 2.04 HS578T_cells, HMEC, A549_cells 111896 R38936 Hs.24894 H sapiens clone 25248 mRNA seq 2.04 HS578T_cells, PC3_cells, 293T_cells 101849 M94167 Hs.172816 neuregulin 1 2.04 HMEC, HS578T_cells, HMEC (total RNA) 119913 W85931 Hs.58785 ESTs 2.04 HMEC, BT474_cells, MB231_cells 130785 AA242826 Hs.19405 caspase recruitment domain 4 2.04 HMEC, HS578T_cells, BT474_cells 124702 R06984 Hs.7745 ESTs; Weakly similar to TESTIS-SPECIFIC 2.03 Fibroblasts 2, PRSC_con, HMEC 105769 AA478001 Hs.225935 diacylglycerol O-acyltransferase (mouse) 2.03 PC3_cells, EB_cells, HS578T_cells 132219 N48682 Hs.172971 ESTs 2.03 HT29_cells, PC3_cells, A549_cells 122033 AA431334 Hs.109297 ESTs 2.03 OVCAR_cells, A549_cells, Caco2 120461 AA251301 zs10b02.s1 NCI_CGAP_GCB1 H sapiens cDNA 2.03 HS578T_cells, EB_cells, EB_cells contains Alu repetitive element;, mRNA 134959 U90550 Hs.91813 butyrophilin; subfamily 2; member A2 2.03 HMEC, Fibroblasts 2, EB_cells 104909 AA055892 Hs.14543 ESTs 2.03 Lu_SC_H345, PC3_cells, DU145_cells 101950 S79219 Hs.80741 propionyl Coenzyme A carboxylase; alpha 2.03 Lu_SC_H69, EB_cells, CALU6_cells 133878 D78947 Hs.7718 ESTs; Weakly similar to weak similarity 2.02 EB_cells, MCF7, MB231_cells 103459 X99894 Hs.32938 insulin promoter factor 1; homeodomain t 2.02 EB_cells, Lu_AD_H23, Lu_AD_358 125507 AI436377 Hs.258590 tetraspanin TM4-B 2.02 A549_cells, Lu_SQ_H520, Lu_AD_H23 116857 F04014 Hs.65996 ESTs 2.01 HS578T_cells, HMEC, MB231_cells 112920 T10234 Hs.4275 ESTs 2.01 HS578T_cells, EB_cells, PRSC_con 105533 AA258572 Hs.6418 ESTs; Moderately similar to seven transm 2.01 HS578T_cells, HMEC, EB_cells 126762 AA064671 zm13b04.r1 Stratagene pancreas (#937208) 2.01 RPWE_2, Lu_AD_H23, Lu_AD_358 similar to TR:G413842 G413842 NONCLASSI 128999 R37808 Hs.107765 ESTs 2.01 HS578T_cells, OVCAR_cells, EB_cells 133902 AA114858 Hs.7745 ESTs; Weakly similar to TESTIS-SPECIFIC 2 Fibrablasts 2, PRSC_con, DU145_cells

[0328] TABLE 2 Pkey: Unique Eos probeset identifier number ExAccn: Exemplar Accession number, Genbank accession number UnigeneID: Unigene number Unigene Title: Unigene gene title Pkey Ex Accn UniG_ID Complete_Title Ratio Mets/BS Top 3 expressing cell lines 101447 M21305 Hs.247946 Human alpha satellite and satellite 3 ju 110.98 EB_cells, Fibroblasts2, A549_cells 105039 AA130349 Hs.36475 ESTs 9.13 EB_cells, OVCAR_cells, Lu_SC_H345 106094 AA419461 Hs.18127 ESTs 8.51 H729_cells, MB-MDA-453, HS578T_cells 105777 AA348412 Hs.23096 ESTs 8.4 293T_cells, OVCAR_cells, EB_cells 129818 N54841 Hs.172572 ESTs 7.2 Lu_SC_H69, EB_cells, Lu_SC_H345 118475 N66845 Hs.165411 ESTs; Weakly similar to !!!! ALU CLASS B 7 DU145_cells, EB₁₃ cells, Caco2 112170 R48744 Hs.192878 ESTs 6.91 293T_cells, DU145_cells, HT29_cells 114918 AA236813 Hs.72324 ESTs; Highly simharto unknown [H.sapie 6.6 EB_cells, 293T_cells, DU145_cells 104590 R79750 Hs.83623 nuclear receptor subfamily 1; group I; m 6.58 293T_cells, OVCAR_cells, HMEC 120625 AA285053 Hs.107168 ESTs 6.55 CALU6_cells, OVCAR_cells, EB_cells 115650 AA404564 Hs.47094 ESTs 6.43 EB_cells, LNCaP_cells, Lu_SC_H345 124568 N67086 Hs.102000 ESTs 6.35 PC3_cells, A549_cells, DU145_cells 134238 R81509 Hs.184571 splicing factor arginine/serine-rich 11 6.32 293T_cells, Lu_SC_H345, HMEC 114721 AA131450 Hs.103822 ESTs 6.13 Caco2, MB-MDA-435s, PRSC_log 106145 AA424791 Hs.5734 KIAA0679 protein 6 OVCAR_cells, EB_cells, 293T_cells 114610 AA081079 zn32h9.s1 Stratagene endothelial cell 93 5.97 PRSC_con, DU145_cells, HS578T_cells IMAGE:549185 3′, mRNA seq 130281 R12777 Hs.15395 ESTs; Weakly similar to ARGINYL-TRNA SYN 5.94 PRSC_con, HT29_cells, EB_cells 124690 R05818 Hs.173830 ESTs 5.92 LNCaP_cells, EB_cells, OVCAR_cells 113490 T88700 Hs.173374 ESTs 5.81 DU145_cells, PC3_cells, HMEC (total RNA) 104425 H88496 Hs.40583 ESTs 5.77 OVCAR_cells, HS578T_cells, A549_cells 118828 N79496 Hs.50824 EST 5.45 LNCaP_cells, OVCAR_cells, DU145_cells 129076 AA262179 Hs.169343 ESTs 5.35 293T_cells, BT474_cells, MCF7 109684 F09317 Hs.140885 ESTs; Weakly similar to LINE-1 REVERSE T 5.34 Fibroblasts 2, Lu_SC_H69, DU145_cells 104558 R56678 Hs.88959 Human DNA seq from clone 967N21 on chr 2 5.32 EB_cells, PC3_cells, Lu_SC_H345 part of KIAA0172; the gene for a novel 109032 AA158234 Hs.72222 ESTs 5.23 HT29_cells, PC3_cells, Lu_AD_358 129350 U50535 Hs.110630 Human BRCA2 region: mRNA seq CG006 5.2 293T_cells, EB_cells, DU145_cells 112662 R85436 Hs.193150 ESTs 5.2 MB-MDA-435s, PRSC_con, MB-MDA-453 132902 AA490969 Hs.168147 ESTs 5.18 PC3_cells, LNCaP_cells, CALU6_cells 126872 AA136653 ESTs 5.04 EB_cells, Fibroblasts 2, A549_cells 122528 AA449804 Hs.250992 EST 5.04 Lu_SC_H345, PRSC_con, LNCaP_cells 102193 U20758 Hs.313 secreted phosphoprotein 1 (osteopontin; 5.02 Lu_LC_H460, A549_cells, MB-MDA-435s 121332 AA404384 Hs.97921 ESTs 5.01 EB₁₃ cells, Lu_SC_H69, DU145_cells 135357 AA235803 Hs.79572 cathepsin D (lysosomal aspartyl protease 4.96 EB_cells, MCF7, DU145_cells 109141 AA176428 Hs.193380 ESTs 4.86 DU145_cells, PC3_cells, PRSC_log 135324 AA082041 Hs.9873 ESTs 4.83 EB_cells, Lu_SC_H345, HS578T_cells 124875 R70506 Hs.207693 ESTs; Weakly similar to !!!! ALU SUBFAMI 4.75 DU145_cells, OVCAR_cells, LNCaP_cells 102380 U40434 Hs.155981 mesothelin 4.71 OVCAR_cells, Lu_AD_H23, RPWE_2 127956 AA826117 Hs.194013 ESTs 4.69 EB_cells, HS578T_cells, DU145_cells 125038 T78089 Hs.168887 ESTs 4.58 OVCAR_cells, 293T_cells, DU145_cells 102515 U52696 Humn adrenal Creb-rp hmlg (Creb-rp), com 4.57 Lu_SC_H345, Lu_SC_H69, HT29_cells 109027 AA157818 Hs.238380 Human endogenous retroviral protease mRN 4.57 PC3_cells, EB_cells, Lu_SQ_H520 115096 AA255991 Hs.175319 ESTs 4.57 OVCAR_cells, 293T_cells, PC3_cells 123470 AA599106 Hs.194208 ESTs 4.55 LNCaP_cells, Lu_SC_H69, 293T_cells 113219 T59257 Hs.194407 ESTs 4.55 A549_cells, 293T_cells, 293T_cells 123433 AA598661 Hs.112478 ESTs 4.55 EB_cells, OVCAR_cells, HT29_cells 135182 M28170 Hs.96023 CD19 antigen 4.53 OVCAR_cells, DU145_cells, EB_cells 121721 AA419470 Hs.199961 ESTs 4.51 DU145_cells, LNCaP_cells, EB_cells 129126 H88486 Hs.108806 ESTs 4.45 LNCaP_cells, Caco2, EB_cells 135232 AA342457 Hs.96800 ESTs; Moderately similar to !!!! ALU SUB 4.43 LNCaP_cells, DU145_cells, OVCAR_cells 124847 R60044 Hs.106706 ESTs; Highly similar to BETA-CATENIN [H. 4.42 OVCAR_cells, CALU6_cells, CALU6_cells 110349 H40988 ESTs; Weakly similar to !!!! ALU SUBFAMI 4.39 DU145_cells, OVCAR_cells, LNCaP_cells 134402 U25165 Hs.82712 fragile X mental retardation; autosomal 4.38 HS578T_cells, OVCAR_cells, DU145_cells 115494 AA290603 Hs.256517 ESTs 4.36 Lu_SC_H345, OVCAR_cells, PC3_cells 119174 R71234 yi54c08.s1 Soares placenta Nb2HP H sapie 4.33 DU145_cells, OVCAR_cells, LNCaP_cells transcript (rRNA); gb:541458 ROD CGMP- BETA-SUBUNIT (HUMAN); contain 121943 AA429265 Hs.126759 ESTs 4.3 EB_cells, HT29_cells, Lu_SC_H69 110856 N33063 Hs.23291 ESTs; Weakly similar to S164 [H.sapiens] 4.28 OVCAR_cells, EB_cells, Lu_SC_H69 102474 U49973 Human Tigger1 transposable element comp 4.28 DU145_cells, LNCaP_cells, OVCAR_cells 123458 AA598963 Hs.112499 KIAA0612 protein 4.27 A549_cells, A549_cells, BT474_cells 116459 AA621399 Hs.64193 ESTs 4.22 Caco2, HS578T_cells, MB-MDA-435s 126301 N62371 Hs.100043 ESTs; Weakly similar to Similar to cutic 4.22 PC3_cells, DU145_cells, Lu_SC_H345 123461 AA598990 Hs.251119 EST 4.22 Lu_SC_H345, Lu_SC_H69, OVCAR_cells 130588 AA287735 Hs.16411 Human DNA seq from done 1189B24 on chro 4.2 EB_cells, LNCaP_cells, MCF7 MLRQ subunit (EC 1.6.5.3; EC 1.6.99.3; Tyrosine-protein Kinase FER (EC 2.7.1.1 125756 W25498 Hs.81634 ATP synthase; H + transporting; mitochond 4.2 HMEC, EB_cells, DU145_cells 135009 AA040507 Hs.251865 ESTs 4.19 293T_cells, EB_cells, DU145_cells 107001 AA598589 Hs.24492 ESTs 4.18 293T_cells, DU145_cells, EB_cells 124896 R82063 Hs.101594 EST 4.16 OVCAR_cells, Lu_SC_H345, HMEC (total RNA) 119404 792950 ye27c10.s1 Stratagene lung (#937210) H s 4.15 DU145_cells, PC3_cells, Fibroblasts 2 125090 T91518 ye20f05.s1 Stratagene lung (#937210) H s 4.14 LNCaP_cells, DU145_cells, OVCAR_cells contains Alu repetitive element; contain 117348 N24157 Hs.139615 ESTs 4.1 Lu_SC_H345, Lu_SC_H69, PRSC_log 111389 N95837 Hs.169111 ESTs; Weakly similar to LB2A [D.melanoga 4.1 DU145_cells, MCF7, LNCaP_cells 134977 AA464698 Hs.19390 ESTs; Weakly similar to bullous pemphigo 4.09 OVCAR_cells, Fibroblasts 2, Lu_SC_H69 124696 R06273 Hs.186467 ESTs; Moderately similar to !!!! ALU SUB 4.09 OVCAR_cells, Lu_SC_H345, PRSC_con 124090 H09570 Hs.143032 ESTs; Weakly similar to neuronal thread 3.98 DU145_cells, OVCAR_cells, Lu_SC_H345 133992 R46354 Hs.169832 zinc finger protein 42 (myeloid-speciflc 3.98 HT29_cells, MB231_cells, BT474_cells 126009 H51652 Hs.242985 hemoglobin; gamma G 3.96 Lu_SC_H69, OVCAR_cells, EB_cells 114161 Z38904 Hs.22385 ESTs; Weakly similar to KIAA0970 protein 3.94 HS578T_cells, EB_cells, PRSC_con 109171 AA180356 Hs.73700 EST 3.94 293T_cells, MB-MDA-435s, A549_cells 122007 AA430629 Hs.98564 ESTs 3.93 PC3_cells, A549_cells, OVCAR_cells 131936 AA094865 Hs.179972 interferon; alpha-inducible protein (clo 3.9 CALU6_cells, EB_cells, Lu_SC_H69 128668 AA194849 Hs.103422 ESTs 3.9 Lu_AD_H23, EB_cells, Lu_SC_H69 124977 T33859 Hs.190452 KIAA0365 gene product 3.89 293T_cells, DU145_cells, EB_cells 107048 AA600012 Hs.10669 ESTs; Moderately similarto KIAA0400 [H. 3.89 PC3_cells, HS578T_cells, DU145_cells 105358 AA236034 Hs.25362 ESTs 3.89 Caco2, EB_cells, CALU6_cells 135106 AA599037 Hs.9456 SWI/SNF related; matrix assocd; actin de 3.86 EB_cells, LNCaP_cells, Caco2 106686 AA463215 Hs.29896 ESTs; Weakly similar to proline-rich pro 3.85 OVCAR_cells, DU145_cells, EB_cells 132093 AA400091 Hs.39421 ESTs 3.85 OVCAR_cells, OVCAR_cells, LNCaP_cells 128651 AA446990 Hs.103135 ESTs 3.84 EB_cells, LNCaP_cells, OVCAR_cells 102459 U48936 Human amiloride-sensitive epithelial sod 3.84 HT29_cells, BT474_cells, Lu_SC_H69 113732 798288 Hs.193295 ESTs; Weakly similar to !!!! ALU SUBFAMI 3.82 DU145_cells, OVCAR_cells, LNCaP_cells 116000 AA448710 Hs.41327 ESTs 3.82 DU145_cells, MB-MDA-453, Lu_SC_H69 120748 AA303153 Hs.237994 EST; Weakly similarto !!!! ALU SUBFAMIL 3.82 DU145_cells, DU145_cells, Lu_SC_H345 116318 AA490830 Hs.58570 deleted in cancer 1; RNA helicase HDB/DI 3.79 MB-MDA-453, CALU6_cells, EB_cells 114366 Z41747 Hs.469 succinate dehydrogenase complex; subunit 3.78 DU145_cells, Fibroblasts 2, Caco2 107248 D59894 Hs.34782 ESTs 3.75 LNCaP_cells, DU145_cells, EB_cells 132713 AA286906 Hs.55335 ESTs 3.75 OVCAR_cells, EB_cells, Lu_SC_H345 102222 U24683 Hs.159386 Immunoglobulin heavy variable 4-4 3.73 EB_cells, OVCAR_cells, 293T_cells 108201 AA057518 Hs.63394 ESTs 3.72 293T_cells, DU145_cells, EB_cells 119940 W86779 Hs.171807 DKFZP586B0319 protein 3.71 EB_cells, Caco2, DU145_cells 106508 AA452590 Hs.30348 ESTs 3.67 EB_cells, LNCaP_cells, 293T_cells 114360 Z41592 Hs.22129 hypothetical protein 3.67 HT29_cells, Lu_SQ_H520, Lu_SQ_H520 100991 J03764 Hs.82085 plasminogen activator inhibitor; type I 3.67 Fibroblasts 2, HS578T_cells, MB231_cells 107580 AA002091 Hs.175476 ESTs; Weakly similar to !!!! ALU SUBFAMI 3.67 OVCAR_cells, LNCaP_cells, Lu_SC_H345 111685 R21408 Hs.106095 ESTs 3.66 OVCAR_cells, A549_cells, 293T_cells 128336 AI242720 Hs.146043 ESTs; Weakly similar to alternatively sp 3.66 Lu_SC_H345, Caco2, OVCAR_cells 130868 AA004900 Hs.171917 ESTs; Weakly similar smlr to glycerophos 3.61 EB_cells, HS578T_cells, LNCaP_cells 116802 H44061 Hs.194026 ESTs 3.6 Lu_SC_H345, OVCAR_cells, DU145_cells 130753 Z46632 Hs.189 phosphodiesterase 40; cAMP-specific (dun 3.6 Lu_SC_H69, Lu_AD_H23, Lu_SC_H345 123074 AA485117 Hs.105653 ESTs 3.6 293T_cells, MB231_cells, Fibroblasts 2 114317 Z41038 Hs.469 succinate dehydrogenase complex; subunit 3.6 DU145_cells, HS578T_cells, CALU6_cells 134194 AA233231 Hs.79828 ESTs 3.59 BT474_cells, MB231_cells, HT29_cells 127752 AA808388 Hs.211167 ESTs 3.59 Lu_SQ_H520, MB-MDA.435s, DU145_cells 123526 AA608657 ESTs; Moderately similar to !!!! ALU SUB 3.59 DU145_cells, OVCAR_cells, LNCaP_cells 127917 AA211895 Hs.118831 EST; Highly similar to dJ1163J1.2.1 [H.s 3.58 Lu_SC_H345, OVCAR_cells, PRSC_con 105941 AA404427 Hs.10669 ESTs; Moderately similar to KIAA0400 [H. 3.58 PC3_cells, DU145_cells, HS578T_cells 124694 R06108 Hs.135258 ESTs 3.56 Lu_AD_H23, Lu_SQ_H520, Lu_AD_358 105658 AA282571 Hs.203772 FSHD region gene 1 3.56 DU145_cells, EB_cells, A549_cells 111168 N66951 Hs.238380 Human endogenous retroviral protease mRN 3.55 PC3_cells, EB_cells, MB231_cells 133254 AA156670 Hs.180780 H sapiens agrin precursor mRNA; partial 3.54 OVCAR_cells, DU145_cells, PC3_cells 132840 U33821 Tax1 (human 7-cell leukemia virus type I 3.53 MB231_cells, CALU6_cells, BT474_cells 116562 D25807 Hs.90145 ESTs 3.52 MB231_cells, BT474_cells, Lu_SC_H345 126045 N80361 Hs.14248 ESTs 3.51 DU145_cells, Lu_SC_H345, OVCAR_cells 122878 AA465341 Hs.99640 ESTs 3.47 HT29_cells, OVCAR_cells, HMEC 105220 AA210695 Hs.17212 ESTs 3.47 MB-MDA-435s, HT29_cells, HT29_cells 127001 AA731636 Hs.59319 ESTs; Weakly similar to !!!! ALU SUBFAMI 3.45 LNCaP_cells, DU145_cells, Lu_SC_H345 112693 R88741 Hs.91065 ESTs; Moderately similar to proliferatio 3.44 EB_cells, LNCaP_cells, DU145_cells 104935 AA063280 Hs.35552 ESTs 3.43 LNCaP_cells, CALU6_cells, 293T_cells 128710 J04813 Hs.104117 cytochrome P450; subfamily IIIA (niphedi 3.41 HT29_cells, A549_cells, Fibroblasts 2 131996 D86956 Hs.36927 heat shock 105 kD 3.4 EB_cells, PC3_cells, Lu_SC_H345 119229 T03229 H sapiens (clone 104) retinoblastoma 1 g 3.4 DU145_cells, Lu_SC_H345, EB_cells 128046 AA873285 Hs.137947 ESTs 3.39 EB_cells, LNCaP_cells, DU145_cells 105175 AA186804 Hs.25740 ESTs; Weakly similar to ubiquitous TPR m 3.39 PC3_cells, MCF7, DU145_cells 132349 Y00705 Hs.181286 serine protease inhibitor; Kazal type 1 3.38 Caco2, EB_cells, Lu_SC_H69 101569 M32053 Human H19 RNA gene, complete cds 3.37 Lu_SC_H69, MCF7, OVCAR_cells 116389 AA599011 troponin T1; skeletal; slow 3.36 DU145_cells, LNCaP_cells, OVCAR_cells 130641 AA182001 Hs.17155 ESTs 3.36 DU145_cells, MB-MDA-435s, HS578T_cells 109362 AA214615 Hs.194348 ESTs 3.33 HT29_cells, Fibroblasts 2, BT474_cells 106278 AA432292 Hs.23388 ESTs; Moderately similar to !!!! ALU SUB 3.33 EB_cells, Fibroblasts 2, BT474_cells 127241 AA321849 Hs.248340 H sapiens mRNA; cDNA DKFZp564J2116 (from 3.32 LNCaP_cells, DU145_cells, EB_cells 133339 N64588 Hs.71252 ESTs 3.32 DU145_cells, EB_cells, Caco2 113260 T64896 Hs.237992 ESTs 3.32 Lu_SQ_H345, LNCaP_cells, Lu_SC_H69 133349 N75791 Hs.7153 L-3-hydroxyacyl-Coenzyme A dehydrogenase 3.31 Caco2, EB_cells, OVCAR_cells 107149 AA621159 Hs.23284 ESTs 3.29 HS578T_coells, DU145_cells, PRSC_con 133195 AA350744 Hs.181409 KIAA1007 protein 3.29 EB_cells, Lu_AD_H23, Lu_AD_358 111302 N73838 Hs.15049 ESTs 3.29 DU145_cells, EB_cells, HS578T_cells 106414 AA447971 Hs.28827 ESTs 3.28 A549_cells, OVCAR_cells, PC3_cells 121768 AA421561 Hs.251664 insulin-like growth factor 2 (somatomedi 3.28 Caco2, PRSC_con, PRSC_log 117176 H98670 Hs.49753 ESTs; Weakly similar to hypothetical pro 3.28 PRSC_log, CALU6_cells, OVCAR_cells 131320 AA171948 Hs.145696 splicing factor(CC1.3) 3.28 EB_cells, LNCaP_cells, DU145_cells 100700 HG3227-H Guanine Nucleotide-Binding Protein Hsr1 3.27 EB_cells, RPWE_2, Lu_AD_H23 134275 AA132328 Hs.3688 acid-inducible phosphoprotein 3.26 EB_cells, DU145_cells, LNCaP_cells 117667 N39214 Hs.44708 Ser-Thr protein kinase related to the my 3.26 LNCaP_cells, DU145_cells, MB-MDA-453 124889 R78604 Hs.101570 ESTs 3.25 Lu_AD_H23, Lu_SC_H69, Lu_SC_H345 126631 W95117 Hs.193337 ESTs 3.25 Lu_SC_H345, OVCAR_cells, Lu_SC_H69 105643 AA282069 Hs.173802 KIAA0603 gene product 3.24 Caco2, EB_cells, 293T_cells 132718 AA056731 Hs.554 Siogren syndrome antigen A2 (60 kD; ribon 3.24 CALU6_cells, OVCAR_cells, A549_cells 116417 AA609309 Hs.239302 ESTs; Weakly similar to !!!! ALU SUBFAMI 3.24 A549_cells, CALU6_cells, 293T_cells 108039 AA041341 Hs.46670 ESTs 3.24 293T_cells, EB₁₃ cells, Caco2 114116 Z38496 Hs.103283 KIAA0594 protein 3.23 DU145_cells, OVCAR_cells, EB_cells 124514 N58045 Hs.142737 ESTs 3.22 EB_cells, Caco2, Lu_SQ_H520 110802 N26651 Hs.252748 ESTs 3.22 LNCaP_cells, MB-MDA-435s, MB-MDA-453 106920 AA490899 Hs.24462 ESTs 3.22 DU145_cells, EB_cells, OVCAR_cells 123523 AA608588 Hs.193634 ESTs 3.21 DU145_cells, LNCaP_cells, OVCAR_cells 131564 AA491465 Hs.28792 ESTs 3.2 HS578T_cells, HMEC (total RNA), HMEC 119423 T99544 Hs.173734 ESTs; Weakly similar to !!!! ALU CLASS B 3.2 EB_cells, DU145_cells, Caco2 128736 F03934 Hs.104607 ESTs 3.19 PC3_cells, Lu_SQ_H520, Lu_SC_H69 101511 M27826 Hs.238380 Human endogenous retroviral protease mRN 3.18 PC3_cells, DU145_cells, Lu_SQ_H520 114509 AA043551 Hs.95249 ESTs 3.18 EB₁₃ cells, Lu_SC_H345, DU145_cells 124196 H52617 Hs.144167 ESTs 3.17 BT474_cells, MB231_cells, HMEC 129095 L12350 Hs.108623 thrombospondin 2 3.17 Fibroblasts 2, PRSC_con, PRSC_log 116457 AA621367 Hs.119683 ESTs 3.17 293T_cells, Lu_SC_H345, CALU6_cells 117040 H89112 yw25e5.s1 Morton Fetal Cochlea H sapiens 3.16 OVCAR_cells, 293T_cells, EB_cells 129112 N32521 Hs.108738 ESTs 3.16 EB_cells, Fibroblasts 2, MB231_cells 130418 J03242 Hs.251664 insulin-like growth factor 2 (somatomedi 3.16 Caco2, PRSC_con, PRSC_log 131199 R80048 Hs.234433 ESTs; Weakly similar to transporter prot 3.15 PC3_cells, EB_cells, OVCAR_cells 110357 H41529 Hs.33549 ESTs; Highly similar to sulfonylurea rec 3.15 Lu_SQ_H345, PRSC_con, Lu_AD_H23 130068 AA608903 Hs.106220 KIAA0336 gene product 3.15 OVCAR_cells, CALU6_cells, HS578T_cells 127423 T47546 Hs.119252 tumor protein; translationally-controlle 3.15 EB_cells, PRSC_con, LNCaP_cells 105028 AA126719 Hs.25282 ESTs 3.14 LNCaP_cells, PC3_cells, EB_cells 102349 U37547 Hs.75263 apoptosis inhibitor 1 3.14 DU145_cells, HS578T_cells, LNCaP_cells 105126 AA157814 Hs.36288 ESTs 3.13 EB_cells, HS578T_cells, LNCaP_cells 115465 AA286941 Hs.43691 ESTs 3.12 EB_cells, DU145_cells, 293T_cells 133240 AA086452 Hs.68731 triadin 3.12 Lu_SQ_H520, Lu_AD_H23, PRSC_log 122698 AA456112 Hs.99410 ESTs 3.12 DU145_cells, OVCAR_cells, A549_cells 123553 AA608841 Hs.111977 ESTs 3.12 EB_cells, Caco2, DU145_cells 133437 R57419 Hs.7370 ESTs 3.11 HS578T_cells, 293T_cells, Caco2 104956 AA074880 Hs.120975 ESTs; Weakly similar to hypothetical pro 3.11 OVCAR_cells, Fibroblasts 2, Caco2 116314 AA490588 Hs.43118 ESTs 3.11 EB_cells, MB-MDA-435s, HT29_cells 120562 AA280036 Hs.173912 eukaryotic translation initiation factor 3.11 LNCaP_cells, DU145_cells, EB_cells 108770 AA127845 Hs.71027 EST 3.11 Lu_LC_H460, Lu_SC_H345, Lu_AD_358 129791 F02778 Hs.173887 KIAA0876 protein 3.1 Lu_SC_H345, Lu_SC_H69, PRSC_log 115783 AA424487 Hs.72289 ESTs; Weakly similar to LIV-1 protein [H 3.09 Lu_AD_358, EB₁₃ cells, PC3_cells 107630 AA007218 Hs.60178 ESTs 3.07 Lu_SC_H345, CALU6_cells, Lu_SC_H69 124339 H99093 Hs.6179 H sapiens mRNA; cDNA DKFZp586K2322 (from 3.07 293T_cells, MB-MDA-453, Caco2 122314 AA442257 Hs.192076 ESTs 3.07 293T_cells, LNCaP_cells, PC3_cells 104589 R79299 Hs.241160 ESTs; Moderately similarto !!!! ALU SUB 3.07 293T_cells, DU145_cells, EB_cells 115687 AA410508 Hs.163765 ESTs; Moderately smlr to ORF derived frm 3.06 Caco2, EB_cells, MB231_cells 123796 AA620390 Hs.247444 ESTs 3.06 Lu_SC_H345, LNCaP_cells, DU145_cells 106483 AA451676 Hs.30299 IGF-II mRNA-binding protein 2 3.06 OVCAR_cells, HMEC (total RNA), HMEC 133318 AA256168 Hs.70838 ESTs 3.05 OVCAR_cells, LNCaP_cells, 293T_cells 117244 N20979 Hs.1757 L1 cell adhesion molecule (hydrocephalus 3.05 MB_cells, MCF7, CALU6_cells thumbs) syndrome; spastic paraplegia 1) 130797 AA430050 Hs.180948 KIAA0729 protein 3.05 EB_cells, DU145_cells, DU145_cells 128959 D79791 Hs.107381 ESTs; Weakly similar to F38A5.1 [C.elega 3.05 LNCaP_cells, HS578T_cells, Lu_SQ_H520 120481 AA252703 Hs.191754 ESTs 3.04 EB_cells, Fibroblasts 2, PRSC_con 126649 AA856990 Hs.125058 ESTs 3.03 OVCAR_cells, LNCaP_cells, 293T_cells 106970 AA504835 Hs.24252 ESTs 3.03 EB_cells, OVCAR_cells, 293T_cells 126488 N34935 Hs.25633 ESts; Highly similar to ARF GTPase-activ 3.03 LU_AD_358, MCF7, MB231_cells 119498 W37226 Hs.55573 ESts 3.01 293T_cells, HS578T_cells, CALU6_cells 129967 H99653 Hs.138618 ESTs 3.01 Lu_SC_H345, Lu_SC_H69, PRSC_log 130698 AA037357 Hs.188212 Ests 3.01 OVCAR_cells, LNCaP_cells, DU145_cells 111018 N54067 Hs.3626 mitogen-activated protein kinase kinase 3.01 PC3_cells, Caco2, Fibroblasts 2 123196 AA489250 Hs.59403 serine palmitoyltransferase; subunit II 3 Lu_SC_H345, BT474_cells, Lu_SC_H69 133229 AA203433 Hs.6834 KIAA1014 protein 3 OVCAR_cells, 293T_cells, EB_cells 130405 H88359 Hs.155396 nuclear factor (erythroid-derived 2)-lik 3 PRSC_con, EB₁₃ cells, DU145_cells 107881 AA025567 Hs.61273 H sapiens chromosome 19; cosmid R32611 3 Lu_SQ_H520, MCF7, Lu_AD_358 116589 D59570 Hs.17132 ESTs 3 EB_cells, A549_cells, HS578T_cells 105479 AA255546 Hs.23467 ESTs 2.99 Lu_SC_H345, PC3_cells, OVCAR_cells 115560 AA393812 Hs.50575 ESTs; Moderately similar to !!!! ALU SUB 2.99 EB_cells, Lu_SC_H69, Fibroblasts 2 130166 AA350690 Hs.151411 KIAA0916 protein 2.98 LNCaP_cells, EB_cells, 293T_cells 123355 AA504773 Hs.160557 ESTs 2.98 PRSC_con, PRSC_log, PRSC_log 109546 F01449 Hs.26954 ESTs 2.97 Lu_SC_H345, HT29_cells, BT474_cells 129001 AA448946 Hs.107812 ESTs; Weakly similar to proline-rich pro 2.97 EB_cells, Lu_AD_H23, Lu_AD_358 102259 U28369 Hs.82222 sema domain; immunoglobulin domain (Ig); 2.97 EB_cells, MB231_cells, OVCAR_cells 105583 AA278907 Hs.24549 ESTs 2.96 EB_cells, DU145_cells, 293T_cells 131859 M90657 Hs.3337 transmembrane 4 superfamily member 1 2.96 A549_cells, PC3_cells, DU145_cells 114533 AA053401 Hs.177526 ESTs 2.96 293T_cells, Lu_LC_H460, PC3_cells 110220 H23543 Hs.27090 ESTs 2.95 PRSC_log, Lu_SC_H345, MB231_cells 124917 R91241 Hs.75470 hypothetical protein; expressed in osteo 2.95 Lu_SC_H345, Lu_SC_H69, PRSC_log 127111 AA805726 Hs.220509 ESTs 2.94 HS578T_cells, 293T_cells, 293T_cells 134882 N73762 Hs.90638 ESTs 2.94 EB_cells, MB-MDA-453, Fibroblasts 2 121788 AA423968 Hs.178113 ESTs; Moderately similar to kinesin like 2.94 HT29_cells, CALU6_cells, HMEC 128530 AA504343 Hs.183475 H sapiens clone 25061 mRNA seq 2.94 DU145_cells, Lu_SC_H345, Caco2 128435 AI301201 Hs.147112 ESTs 2.93 EB_cells, Lu_SQ_H520, PRSC_con 113782 W15580 Hs.15342 phosphate cytidylyltransferase 1; cholin 2.93 EB_cells, Lu_AD_H23, PRSC_log 127569 AA588536 Hs.191783 ESTs 2.93 EB_cells, HS578T_cells, Lu_AD_358 109642 F04465 Hs.22394 ESTs; Weakly similar to weak similarity 2.92 PC3_cells, EB_cells, OVCAR_cells protein US)1 [C.elegans] 114615 AA083812 Hs.159456 DKFZP566F123 protein 2.92 A549_cells, HS578T_cells, PRSC_con 126808 AA086320 zn52d12.s1 Stratagene muscle 937209 H sa 2.92 Lu_SC_H69, Lu_SC_H345, EB_cells 113947 W84768 Hs.141742 ESTs 2.92 DU145_cells, Fibroblasts 2, MCF7 129455 W27301 Hs.187991 DKFZPS64A122 protein 2.91 OVCAR_cells, DU145_cells, CALU6_cells 107772 AA018587 Hs.40515 ESTs; Weakly similar to !!!! ALU SUBFAMI 2.91 OVCAR_cells, EB_cells, PC3_cells 127159 AA284097 Hs.237955 RAB7; member RAS oncogene family 2.91 293T_cells, OVCAR_cells, PC3_cells 124792 R44357 Hs.132784 ESTs; Weakly similar to cDNA EST EMBL:T0 2.91 DU145_cells, DU145_cells, CALU6_cells 109751 F10210 Hs.6679 H sapiens mRNA; cDNA DKFZp586A0424 (from 2.91 EB_cells, Lu_SC_H69, 293T_cells 128926 AA481403 Hs.107213 ESTs; Highly similar to NY-REN-6 antigen 2.9 CALU6_cells, EB_cells, OVCAR_cells 106637 AA459961 Hs.250824 ESTs 2.9 EB_cells, Caco2, MB-MDA-435s 132164 U84573 Hs.41270 procollagen-lysine; 2-oxoglutarate 5-dio 2.9 DU145_cells, HS578T_cells, A549_cells 128099 AA905327 ESTs 2.9 MCF7, HMEC (total RNA), 293T_cells 104818 AA034947 Hs.24831 ESTs 2.9 EB_cells, Lu_LC_H460, 293T_cells 126050 H27267 Hs.75860 hydroxyacyl-Coenzyme A dehydrogenase/3-k 2.89 LNCaP_cells, DU145_cells, OVCAR_cells -Coenzyme A hydratase (trifunctional pro 116696 F09780 Hs.66124 EST 2.89 CALU6_cells, 293T_cells, 293T_cells 135204 AA421146 Hs.183418 cell division cycle 2-like 1 (PITSLRE pr 2.89 PC3_cells, EB_cells, LNCaP_cells 134946 AA406534 Hs.193053 ESTs; Weakly similar to hiwi [H.sapiens] 2.88 EB_cells, LNCaP_cells, Caco2 114975 AA250850 Hs.13944 adrenergic; beta; receptor kinase 2 2.88 EB_cells, EB_cells, EB_cells 113792 W35212 Hs.17691 ESTs; Weakly similar to env protein [H.s 2.88 MB-MDA-435s, Lu_SC_H69, CALU6_cells 102322 U34962 Hs.54473 cardiac-specific homeo box 2.88 293T_cells, HT29_cells, Lu_AD_H23 125642 AI096849 Hs.25274 ESTs; Moderately similar to putative sev 2.88 PC3_cells, CALU6_cells, 293T_cells 100288 D43951 Hs.153834 Human mRNA for KIAA0099 gene; complete c 2.88 293T_cells, LNCaP_cells, EB_cells 105878 AA400184 Hs.24656 KIAA0907 protein 2.88 OVCAR_cells, DU145_cells, 293T_cells 125262 W88755 Hs.108514 ESTs; Highly similar to Trio [H.sapiens] 2.88 DU145_cells, HS578T_cells, MB231_cells 114419 AA011448 Hs.106532 ESTs; Weakly similar to transposon LRE2 2.88 EB_cells, Lu_AD_H23, Fibroblasts 2 130639 D59711 Hs.17132 ESTs 2.87 EB_cells, A549_cells, OVCAR_cells 130972 AA370302 Hs.21739 H sapiens mRNA; cDNA DKFZp586I1518 (from 2.87 293T_cells, A549_cells, Lu_LC_H460 126906 H66949 Hs.168069 ESTs; Highly similar to CALCIUM-BINDING 2.87 Lu_SC_H345, Lu_SC_H69, LNCaP_cells 121807 AA424507 Hs.247478 H sapiens Mut S homolog 5 gene; partial 2.87 Lu_SC_H69, HT29_cells, RPWE_2 1C7; LST-1; lymphotoxin beta; tumor necr 105474 AA255440 Hs.219614 F-box protein FBL11 2.87 Lu_AD_H23, Caco2, EB_cells 122348 AA443695 Hs.231476 ESTs 2.87 HT29_cells, Lu_SC_H69, BT474_cells 116368 AA521186 Hs.94217 ESTs 2.86 MB-MDA-453, OVCAR_cells, Lu_SC_H69 135143 AA102644 Hs.69559 KIAA1096 protein 2.86 PC3_cells, EB_cells, 293T_cells 106711 AA464741 Hs.143187 Human DNA from chromosome 19-specific co 2.86 EB_cells, Lu_AD_H23, Lu_LC_H460 128583 L32832 Hs.101842 AT-binding transcription factor 1 2.85 LNCaP_cells, Caco2, EB_cells 132139 AA213410 Hs.111554 ADP-ribosylation factor-like 7 2.85 A549_cells, HS578T_cells, Caco2 114484 AA034378 Hs.252351 HERV-H LTR-associating 2 2.85 PC3_cells, Lu_SQ_H520, MB231_cells 124620 N74051 Hs.194092 ESTs; Weakly similar to !!!! ALU SUBFAMI 2.85 Lu_SC_H345, MB231_cells, Fibroblasts 2 100403 D85527 H sapiens mRNA for LIM domain, partial c 2.84 Lu_AD_358, Lu_AD_358, MB231_cells 129795 AA448627 Hs.125163 ESTs; Weakly similar to !!!! ALU SUBFAMI 2.84 Lu_SC_H345, OVCAR_cells, PC3_cells 128258 T70214 Hs.183548 ESTs 2.84 DU145_cells, DU145_cells, OVCAR_cells 102662 U70321 Hs.130227 tumor necrosis factor receptor superfami 2.84 EB_cells, Lu_AD_H23, Fibroblasts 2 132232 AA252030 Hs.42640 ESTs 2.84 EB_cells, OVCAR_cells, Lu_SC_H345 106111 AA421638 Hs.6451 ESTs 2.83 EB_cells, Lu_LC_H460, OVCAR_cells 123963 C13961 Hs.210115 EST 2.83 DU145_cells, LNCaP_cells, Lu_SC_H345 122783 AA459895 Hs.98988 ESTs 2.83 EB_cells, MCF7, Lu_SC_H69 112788 R96586 Hs.163630 ESTs 2.82 DU145_cells, Lu_SC_H345, EB_cells 120823 AA347546 Hs.185780 ESTs 2.82 HT29_cells, HMEC (total RNA), BT474_cells 100378 D80009 Hs.10848 KIAA0187 gene product 2.82 Caco2, PC3_cells, OVCAR_cells 114677 AA114163 Hs.188877 ESTs 2.81 DU145_cells, MCF7, EB_cells 108085 AA045602 Hs.62863 ESTs; Moderately similar to senne/threo 2.81 EB_cells, Lu_AD_H23, HT29_cells 104938 AA064627 Hs.18341 ESTs; Highly similar to CGI-72 protein [ 2.81 PC3_cells, HS578T_cells, OVCAR_cells 128743 AA237013 Hs.2730 heterogeneous nuclear ribonucleoprotein 2.8 OVCAR_cells, LNCaP_cells, Caco2 124314 H94877 Hs.215766 GTP-binding protein 2.8 LNCaP_cells, DU145_cells, Caco2 134227 D79986 Hs.80338 KIAA0164 gene product 2.8 LNCaP_cells, A549_cells, EB_cells 122922 AA476268 zw44h1.s1 Soares_total_fetus_Nb2HF8_9w H 2.79 Lu_SC_H345, OVCAR_cells, Lu_SC_H69 contains Alu repetitive element; contain 128096 H42968 Hs.155606 paired mesoderm homeo box 1 2.78 Lu_AD_H23, Lu_SC_H69, Lu_LC_H460 129295 AA424782 Hs.110121 SEC7 homolog 2.78 Lu_AD_H23, EB_cells, Lu_SC_H345 116155 AA460957 Hs.76053 DEAD/H (Asp-Glu-Ala-Asp/His) box polypep 2.78 EB_cells, OVCAR_cells, 293T_cells 105911 AA401809 Hs.189910 ESTs 2.77 293T_cells, HS578T_cells, DU145_cells 119232 T03475 Hs.258624 EST 2.77 EB_cells, Lu_AD_H23, Lu_AD_358 131168 AA482007 Hs.23788 ESTs; Weakly similar to homology with is 2.77 EB_cells, Lu_LC_H460, MCF7 106048 AA416697 Hs.15330 ESTs 2.76 OVCAR_cells, Lu_SC_H345, 293T_cells 124352 N21626 Hs.102406 ESTs 2.76 MCF7, MB-MDA-453, CALU6_cells 129349 D86974 Hs.110613 KIAA0220 protein 2.76 DU145_cells, HT29_cells, Lu_SC_H69 106120 AA423808 Hs.8765 RNA helicase-related protein 2.76 OVCAR_cells, EB_cells, 293T_cells 100643 HG2755-H T-Plastin 2.75 293T_cells, PC3_cells, HS578T_cells 128500 U60521 Hs.100641 caspase 9; apoptosis-releted cysteine pr 2.75 Lu_AD_358, Lu_SC_H69, Lu_SC_H345 126090 R44789 Hs.119486 ESTs; Weakly similar to rostral cerebell 2.75 Lu_SC_H69, Lu_SC_H345, BT474_cells 127064 Z43709 HSC1JA091 normalized infant brain cDNA H 2.75 Caco2, A549_cells, HT29_cells 132989 AA480074 Hs.394 adrenomedullin 2.75 EB_cells, OVCAR_cells, DU145_cells 108888 AA135606 Hs.189384 ESTs; Weakly similar to !!!! ALU SUBFAMI 2.75 OVCAR_cells, LNCaP_cells, DU145_cells 119579 W42429 Hs.150607 ESTs 2.74 293T_cells, DU145_cells, PC3_cells 100387 D83777 Hs.75137 KIAA0193 gene product 2.74 CALU6_cells, DU145_cells, Caco2 114744 AA135407 Hs.252351 HERV-H LTR-associating 2 2.74 PC3_cells, Lu_SQ_H520, RPWE_2 129092 AA011243 Hs.63525 poly(rC)-binding protein 2 2.74 EB_cells, MCF7, DU145_cells 125360 AA677978 Hs.189741 ESTs 2.74 Lu_AD_358, Lu_AD_358, PRSC_log 107874 AA025305 Hs.25218 ESTs; Weakly similar to reverse transcti 2.74 Lu_SC_H345, Lu_LC_H460, HT29_cells 114086 Z38266 Hs.12770 H sapiens PAC done DJ0777O23 from 7p14- 2.74 EB_cells, LNCaP_cells, BT474_cells 116180 AA463902 Hs.94964 ESTs 2.73 Lu_SC_H69, PRSC_con, Lu_AD_H23 126027 M61982 ESTs 2.73 LNCaP_cells, DU145_cells, A549_cells 116339 AA496257 Hs.72165 ESTs; Weakly similar to R26984_1 [H.sapi 2.73 EB_cells, DU145_cells, OVCAR_cells 105387 AA236951 Hs.108636 chromosome 1 open reading frame 9 2.72 PC3_cells, EB_cells, Caco2 111359 N91273 Hs.27179 ESTs 2.72 EB_cells, LNCaP_cells, 293T_cells 106680 AA461458 Hs.24789 ESTs 2.72 PC3_cells, Lu_SC_H345, Caco2 118598 N69136 Hs.214343 ESTs 2.72 MB-MDA-453, 293T_cells, BT474_cells 107913 AA027161 Hs.59523 ESTs; Highly similar to G1 TO S PHASE TR 2.71 EB_cells, MCF7, Lu_SC_H345 134315 AA136269 Hs.81648 ESTs; Weakly similar to S164 [H.sapiens] 2.71 EB_cells, DU145_cells, HMEC 135233 AA127463 Hs.9683 protein-kinase; interferon-inducible dou 2.71 EB₁₃ cells, OVCAR_cells, Caco2 112932 T15470 Hs.189810 ESTs 2.7 293T_cells, Lu_AD_H23, PC3_cells 119053 R11501 yf28f1.s1 Soares fetal liver spleen 1NFL 2.7 Lu_SC_H345, Lu_SC_H69, DU145_cells contains Alu repetitive element; mRNA 131206 AA044078 Hs.24210 ESTs 2.7 Caco2, Lu_SC_H345, HS578T_cells 126759 AA063642 ESTs; Highly similar to (defline not ava 2.7 LNCaP_cells, Lu_SC_H345, LuSC_H69 131060 AA160890 Hs.22564 myosin VI 2.7 LNCaP_cells, MCF7, HT29_cells 132135 N69101 Hs.40730 ESTs 2.7 EB_cells, 293T_cells, OVCAR_cells 120835 AA348446 Hs.96906 ESTs 2.7 Fibroblasts 2, CALU6_cells, RPWE_2 113815 W45311 Hs.14756 ESTs 2.7 EB_cells, PC3_cells, DU145_cells 133234 T90092 Hs.6853 ESTs; Weakly similar to !!!! ALU SUBFAMI 2.69 Lu_SC_H345, OVCAR_cells, DU145_cells 126819 AA305536 Hs.161489 ESTs 2.69 EB_cells, DU145_cells, Caco2 125198 W69474 Hs.225550 ESTs 2.69 Lu_SC_H345, Lu_AD_H23, Lu_AD_H23 108394 AA075144 zm86f6.s1 Stratagene ovarian cancer (#93 2.69 HMEC, HMEC (total RNA), Fibroblasts 2 gb:X1664 TRANSLATIONALLY CONTROLLED TUM 134456 X59405 Hs.83532 membrane cofactor protein (CD46; trophob 2.69 EB_cells, LNCaP_cells, DU145_cells 111720 R23739 Hs.23585 KIAA1078 protein 2.88 PC3_cells, HMEC (total RNA), OVCAR_cells 114617 AA084148 Hs.110659 ESTs 2.68 DU145_cells, LNCaP_cells, OVCAR_cells 127787 AA731764 ESTs; Weakly similar to !!!! ALU CLASS C 2.68 HT29_cells, Lu_SC_H345, MB231_cells 101437 M20681 Hs.7594 solute carrier family 2 (facilitated glu 2.68 Caco2, Lu_LC_H460, Fibroblasts 2 133761 AA477223 Hs.75922 brain protein I3 2.68 EB_cells, Lu_AD_H23, Lu_SC_H345 105869 AA399574 Hs.19086 ESTs 2.68 PC3_cells, MCF7, MB231_cells 125191 W67257 Hs.138871 ESTs; Weakly similar to !!!! ALU CLASS B 2.88 OVCAR_cells, DU145_cells, LNCaP_cells 116238 AA479352 Hs.47144 DKFZP586N0819 protein 2.67 OVCAR_cells, DU145_cells, LNCaP_cells 124770 R40555 Hs.120429 ESTs 2.67 Lu_AD_H23, Lu_SC_H69, PRSC_con 101764 M80563 Hs.81256 S100 calcium-binding protein A4 (calcium 2.67 A549_cells, MB231_cells, OVCAR_cells murine placental homolog) 130897 AA063428 Hs.21022 adaptor-related protein complex 3; beta 2.67 EB_cells, Lu_AD_H23, HMEC 133303 H61048 Hs.237352 EST 2.66 Lu_SC_H345, Lu_SC_H69, PRSC_con 124724 R12405 Hs.112423 H sapiens mRNA; cDNA DKFZpS86I1420 (from 2.66 Lu_SC_H345, BT474_cells, OVCAR_cells 123697 AA609601 Hs.221224 ESTs 2.66 OVCAR_cells, 293T_cells, Lu_SC_H69 111548 R09170 Hs.258707 ESTs 2.66 293T_cells, CALU6_cells, A549_cells 107005 AA598679 Hs.194215 ESTs 2.66 Lu_SC_H345, OVCAR_cells, Lu_AD_H23 105569 AA278399 Hs.20596 ESTs 2.65 MCF7, HT29_cells, BT474_cells 132687 AB002301 Hs.54985 KIAA0303 protein 2.65 HMEC (total RNA), HMEC, LNCaP_cells 104105 AA422123 Hs.42457 ESTs 2.65 Lu_SC_H345, Lu_SC_H69, DU145_cells 121335 AA404418 Hs.144953 ESTs 2.65 EB_cells, Fibroblasts 2, DU145_cells 124853 R61693 Hs.172330 ESTs; Weakly similar to Wiskott-Aldrich 2.64 Lu_SC_H69, 293T_cells, EB_cells 124253 H69742 Hs.102201 ESTs 2.64 DU145_cells, OVCAR_cells, Lu_SC_H345 123044 AA481549 Hs.165694 ESTs 2.64 EB_cells, Lu_SC_H69, Lu_SC_H345 129535 AA608852 Hs.112603 EST 2.64 EB_cells, Lu_AD_H23, Fibroblasts 2 131397 AB002336 Hs.26395 erythrocyte membrane protein band 4.1-li 2.64 EB_cells, DU145_cells, Caco2 130175 X75593 Hs.151536 RAB13; member RAS oncogene family 2.64 Fibroblasts 2, PRSC_con, HS578T_cells 127507 AI188445 Hs.152618 ESTs 2.63 EB_cells, Lu_AD_H23, Lu_LC_H460 105377 AA236702 Hs.24371 ESTs 2.63 Caco2, EB₁₃ cells, CALU6_cells 114671 AA112679 Hs.252291 ESTs; Weakly similar to !!!! ALU SUBFAMI 2.63 EB_cells, DU145_cells, Caco2 133726 W19983 Hs.75761 SFRS protein kinase 1 2.63 EB_cells, Lu_AD_H23, Lu_SC_H69 132380 H68018 yr76h05.r1 Soares fetal liver spleen 1NF 2.62 EB₁₃ cells, Lu_AD_H23, Lu_SC_H69 IMAGE:211257 5′, mRNA seq. 127986 AI370418 Hs.192050 ESTs; Weakly similar to !!!! ALU CLASS A 2.62 DU145_cells, OVCAR_cells, LNCaP_cells 116208 AA476333 Hs.42532 ESTs 2.61 DU145_cells, PRSC_con, Fibroblasts 2 130946 AA069456 Hs.21490 KIAA0438 gene product 2.6 LNCaP_cells, DU145_cells, HS578T_cells 106687 AA463234 Hs.119387 KIAA0792 gene product 2.59 EB₁₃ cells, MB-MDA-453, Caco2 101551 M31606 Hs.196177 phosphorylase kinase; gamma 2 (testis) 2.59 LNCaP_cells, EB_cells, MB-MDA-453 114479 AA032084 Hs.124841 ESTs; Moderately similar to transformati 2.59 DU145_cells, Caco2, OVCAR_cells 111863 R37495 Hs.23578 ESTs 2.59 HT29_cells, MB231_cells, Lu_SQ_H520 129018 AA029973 Hs.107979 small membrane protein 1 2.59 A549_cells, EB_cells, HS578T_cells 107058 AA600357 Hs.239409 TIA1 cytotoxic granule-associated RNA-bi 2.58 DU145_cells, Lu_SC_H345, EB_cells 126175 AA056181 Hs.17311 DKFZP434N161 protein 2.58 Lu_SC_H345, DU145_cells, LNCaP_cells 131979 D52154 Hs.172458 iduronate 2-sulfatase (Hunter syndrome) 2.58 DU145_cells, PC3_cells, A549_cells 126122 H80181 ESTs 2.58 DU145_cells, OVCAR_cells, LNCaP_cells 106961 AA504110 Hs.18063 ESTs 2.58 HMEC, DU145_cells, DU145_cells 114730 AA133527 Hs.126925 ESTs; Weakly similar to The K1AA0138 gen 2.58 DU145_cells, LNCaP_cells, MCF7 117342 N24020 Hs.132913 ESTs 2.58 HS578T_cells, DU145_cells, LNCaP_cells 131622 AA424813 Hs.29692 ESTs 2.57 PRSC_con, PRSC_log, HS578T_cells 104904 AA055560 Hs.13179 ESTs; Moderately similar to !!!! ALU SUB 2.57 Lu_SC_H345, Lu_SC_H69, BT474_cells 117359 N24848 Hs.114062 ESTs; Weakly similar to T15B7.2 [C.elega 2.57 HS578T_cells, PRSC_con, EB_cells 123331 AA497013 Hs.188740 ESTs; Weakly similar to !!!! ALU SUBFAMI 2.57 Lu_SC_H69, Caco2, PRSC_con 125324 R07785 yf15c06.r1 Soares fetal liver spleen 1NF 2.57 EB_cells, Lu_AD_H23, Fibroblasts 2 contains Alu repetitive element; contain 129813 T33462 Hs.12600 ESTs 2.57 Lu_SC_H345, 293T_cells, Lu_SC_H69 100265 D38521 Hs.75935 KIAA0077 protein 2.57 EB_cells, LNCaP_cells, PC3_cells 134890 T40902 Hs.90786 ATP-binding cassette; sub-family C (CFTR 2.57 A549_cells, DU145_cells, EB_cells 133582 AA421874 Hs.75087 Fas-activated serine/threonine kinase 2.56 EB_cells, Lu_AD_H123, Lu_AD_358 135011 H73161 Hs.92991 ESTs; Weakly similar to C13F10.4 [C.eleg 2.56 EB_cells, LNCaP_cells, MB-MDA-453 107226 D58185 Hs.21945 ESTs 2.56 Lu_SC_H345, Lu_SC_H69, HMEC (total RNA) 126042 H62441 Hs.157082 H sapiens PAC clone DJ0988G15 from 7q33- 2.56 HMEC (total RNA), HMEC, RPWE_2 114472 AA028924 Hs.177407 ESTs; Weakly similar to !!!! ALU SUBFAMI 2.56 Lu_SC_H345, Lu_SC_H69, DU145_cells 126291 N42090 yy05b07.r1 Soares melanocyte 2NbHM H sap 2.56 HMEC, HMEC (total RNA), PC3_cells 113349 T79021 Hs.14438 ESTs; Moderately similar to histamine N- 2.56 HT29_cells, PRSC_log, Lu_SC_H345 105789 AA347485 Hs.25477 ESTs; Moderately similar to rig-1 protel 2.56 Lu_AD_H23, RPWE_2, Lu_SQ_H520 110918 N46423 Hs.24283 ESTs 2.56 EB_cells, CALU6_cells, DU145_cells 117170 H98153 Hs.42500 ADP-ribosylation factor-like 5 2.56 OVCAR_cells, EB_cells, LNCaP_cells 105159 AA173981 Hs.30490 CD2-associated protein 2.55 LNCaP_cells, EB_cells, DU145_cells 105726 AA292328 Hs.9754 activating transcription factor 5 2.55 MCF7, EB_cells, MB-MDA-453 132079 H67964 Hs.38694 ESTs 2.55 EB_cells, DU145_cells, HS578T_cells 131813 X51757 Hs.3268 heat shock 70 kD protein 6 (HSP70B′) 2.55 Lu_AD_H23, MB231_cells, Fibroblasts 2 133538 L14837 Hs.74614 tight junction protein 1 (zona occludens 2.54 DU145_cells, Caco2, A549_cells 124981 T40849 Hs.114034 maternal G10 transcript 2.54 EB_cells, Caco2, LNCaP_cells 122028 AA431306 Hs.98722 ESTs 2.54 Fibroblasts 2, BT474_cells, HMEC (total RNA) 122487 AA448332 Hs.80598 transcription elongation factor A (SII); 2.54 Lu_SC_H345, MCF7, MB-MDA-453 119315 T41152 Hs.90485 ESTs 2.54 Lu_SC_H345, MB-MDA-435s, PRSC_con 107957 AA031948 Hs.57548 ESTs 2.54 A549_cells, RPWE_2, DU145_cells 122457 AA447780 Hs.96418 ESTs 2.54 DU145_cells, EB_cells, A549_cells 103572 Z25749 Hs.75538 ribosomal protein S7 2.54 EB_cells, CALU6_cells, DU145_cells 124395 N29963 Hs.193977 ESTs 2.54 HMEC (total RNA), HMEC, RPWE_2 116024 AA451748 Hs.83883 Human DNA seq from clone 718J7 on chromo 2.53 LNCaP_cells, RPWE_2, MB-MDA-453 phosphoenolpyruvate carboxykinase 1; ES 134361 D43682 Hs.82208 acyl-Coenzyme A dehydrogenase; very long 2.63 LNCaP_cells, CALU6_cells, DU145_cells 130420 U60975 Human hybrid receptor gp25 precursor mRN 2.53 EB_cells, HMEC (total RNA), Caco2 100336 D63478 Hs.8127 KIAA0144 gene product 2.53 BT474_cells, HT29_cells, Lu_AD_358 105519 AA258063 Hs.23438 ESTs 2.53 EB_cells, Caco2, MB-MDA-435s 124684 R02401 Hs.221078 ESTs 2.53 Lu_SC_H345, OVCAR_cells, Lu_SC_H69 105852 AA398933 Hs.172613 solute carrier family 12 (potassium/chlo 2.52 LNCaP_cells, DU145_cells, EB_cells 105012 AA116036 Hs.9329 chromosome 20 open reading frame 1 2.52 CALU6_cells, Caco2, DU145_cells 126534 W39128 Hs.247901 Human DNA seq from clone 8B1 on chromoso 2.52 BT474_cells, LNCaP_cells, Lu_AD_H23 -CELL MEMBRANE GLYCOPROTEIN PC-1; the ge 135334 AA053134 Hs.241558 ariadne-2 (D. melanogaster) homolog (all 2.52 293T_cells, CALU6_cells, DU145_cells 128538 R44214 Hs.101189 ESTs 2.52 EB_cells, Lu_AD_H23, Lu_SC_H345 109865 H02566 Hs.191268 H sapiens mRNA; cDNA DKFZp434N174 (from 2.52 DU145_cells, LNCaP_cells, OVCAR_cells 118579 N68905 small inducible cytokine A5 (RANTES) 2.51 Lu_SC_H345, LNCaP_cells, Lu_SC_H69 117590 N34904 ESTs; Moderately similarto !!!! ALU SUB 2.51 Lu_SC_H345, DU145_cells, Lu_SC_H69 104340 F15201 ESTs 2.51 Lu_SC_H345, PRSC_con, PRSC_log 122455 AA447744 Hs.99141 EST 2.51 Caco2, Lu_SC_H69, 293T_cells 109339 AA211901 Hs.86430 ESTs 2.51 EB_cells, DU145_cells, CALU6_cells 123258 AA490929 Hs.105274 ESTs 2.51 EB_cells, Lu_AD_H23, Lu_SC_H69 118467 N66763 Hs.43080 ESTs 2.51 CALU6_cells, HS578T_cells, OVCAR_cells 106044 AA416548 Hs.149436 kinesin family member 5B 2.51 EB_cells, Caco2, DU145_cells 107480 W58057 Hs.74304 periplakin 2.5 Caco2, OVCAR_ceUs, HMEC (total RNA) 111760 R26892 Hs.221434 ESTs 2.5 Lu_AD_H23, EB_cells, Lu_AD_358 132474 N68018 Hs.180930 TBP-associated factor 172 2.5 LNCaP_cells, EB_cells, DU145_cells 103423 X97249 Hs.123122 FSH primary response (LRPR1; rat) homolo 2.5 HS578T_cells, Lu_SC_H345, PC3_cells 123488 AA599708 Hs.187764 ESTs; Weakly similar to !!!! ALU SUBEAMI 2.49 OVCAR_cells, Lu_SC_H345, DU145_cells 100475 D90276 Hs.12 carcincembryonic antigen-related cell ad 2.49 MB-MDA-453, 293T_cells, CALU6_cells 112003 R42547 Hs.172551 ESTs 2.49 EB_cells, Lu_AD_H23, Lu_SC_H345 114315 Z41027 Hs.26297 ESTs 2.49 Lu_SC_H69, OVCAR_cells, Lu_AD_H23 105291 AA233311 Hs.28752 ESTs 2.49 EB_cells, CALU6_cells, DU145_cells 135354 AA188934 Hs.99367 ESTs 2.49 MB-MDA-453, Lu_SC_H69, 293T_cells 107521 X78262 H.sapiens mRNA for TRE5 2.49 Lu_SC_H345, Lu_SC_H69, PRSC_con 108373 AA074393 Hs.61950 ESTs: Weakly similar to nuclear protein 2.49 MCF7, MB-MDA-453, Lu_SC_H345 108836 AA132061 Hs.222727 ESTs; Weakly similar to ubiquitous TPR m 2.48 DU145_cells, Lu_SC_H345, Lu_SC_H345 110386 H45516 Hs.33268 ESTs 2.48 PC3_cells, OVCAR_cells, Lu_SQ_Y520 129658 M22348 Hs.131255 ubiquinol-cytochrome c reductase binding 2.48 LNCaP_cells, CALU6_cells, PC3_cells 134283 H12661 Hs.8107 H sapiens mRNA; cDNA DKFZpS86B0918 (from 2.48 HMEC (total RNA), HS578T_cells, HMEC 101844 M93425 Hs.62 protein tyrosine phosphatase; non-recept 2.48 DU145_cells, EB_cells, CALU6_cells 133461 M33318 Hs.183584 cytochrome P450; subfamily IIA (phenobar 2.48 EB_cells, Lu_AD_H23, Lu_AD_358 103545 Z14000 Hs.35384 ring finger protein 1 2.47 HT29_cells, Lu_SQ_H520, BT474_cells 128440 N76763 ESTs 2.47 EB_cells, Lu_AD_H23, Lu_AD_358 134992 H05625 Hs.92414 ESTs 2.47 Lu_SC_H345, CALU6_cells, Lu_SC_H69 116295 AA489016 Hs.91216 ESTs; Highly similar to partial CDS; hum 2.47 MB-MDA-453, 293T_cells, MB-MDA-435s 107004 AA598675 Hs.239475 ESTs 2.47 LNCaP_cells, Cace2, OVCAR_cells 132137 AA282312 Hs.4076 CTD (carboxy-terminal domain; RNA polyme 2.46 Lu_SC_H69, HMEC, EB_cells 126390 W28286 Hs.100090 tetraspan 3 2.46 EB_cells, DU145_cells, LNCaP_cells 113050 T26366 Hs.22711 EST; Weakly similar to 60S RIBOSOMAL PRO 2.46 Lu_LC_H460, EB_cells, Lu_AD_358 101667 M60858 Hs.79110 nucleolin 2.46 PC3_cells, 293T_cells, A549_cells 108569 AA085398 zn7e3.s1 Stratagene hNT neuron (#937233) 2.45 HT29_cells, BT474_cells, Lu_SQ_H520 IMAGE:546748 3′, mRNA seq 117186 H98988 Hs.42612 ESTs 2.45 EB_cells, Lu_AD_H23, Lu_AD_358 129091 AA044622 Hs.183755 Human Chromosome 16 BAG clone CIT987SK-A 2.45 EB_cells, Lu_AD_H23, Lu_AD_H23 128468 T23625 Hs.258674 EST 2.45 Lu_AD_H23, EB_cells, Lu_SC_H69 117498 N31726 Hs.44268 ESTs; Highly similar to myelin gene expr 2.45 Lu_SC_H69, DU145_cells, OVCAR_cells 105407 AA243478 Hs.5206 ESTs 2.45 EB_cells, 293T_cells, PC3_cells 128941 R55763 Hs.107287 ESTs 2.44 EB_cells, LNCaP_cehls, A549_cells 116486 C14128 Hs.251980 EST 2.44 MB-MDA-435s, HS578T_cells, 293T_cells 134869 T35288 Hs.90421 ESTs; Moderately similar to !!!! ALU SUB 2.44 EB_cells, Lu_AD_H23, Lu_AD_358 130664 R09049 Hs.17625 ESTs 2.44 PC3_cells, EB_cells, A549_cells 107985 AA035638 Hs.71968 H sapiens mRNA; cDNA DKFZpS54F053 (from 2.44 PRSC_con, PRSC_log, Caco2 110300 H37820 Hs.124147 ESTs 2.44 MB-MDA-453, Caco2, OVCAR_cells 113471 T87174 Hs.16341 ESTs; Moderately similar to !!!! ALU SUB 2.44 Caco2, OVCAR_cells, LNCaP_cells 131474 U28749 Hs.2726 high-mobility group (nonhistone chromoso 2.44 CALU6_cells, OVCAR_cells, 293T_cells 120791 AA342802 Hs.194031 ESTs 2.44 Lu_AD_H23, Lu_SQ_H520, PRSC_con 133733 AA416973 Hs.75798 Human DNA seq from clone 1183I21 on chro 2.43 EB_cells, Caco2, DU145_cells to predicted fly and worm proteins. Con 119977 W88579 Hs.124744 ESTs 2.43 HT_cells, HMEC (total RNA), HMEC 134921 W60186 Hs.169487 Kreisler (mouse) maf-related leucine zip 2.43 LNCaP_cells, HS578T_cells, MB-MDA-453 132295 H66351 Hs.181042 Dmx-hike 1 2.43 Lu_SC_H69, BT474_cells, Lu_SQ_H520 133395 AA491296 Hs.72805 ESTs 2.43 EB_cells, LNCaP_cells, OVCAR_cells 106728 AA465355 Hs.153768 U3 snoRNP-associated 55-kDa protein 2.43 EB_cells, Lu_AD_H23, PC3_cells 116370 AA521256 Hs.236204 ESTs; Moderately similar to NUCLEAR PORE 2.43 EB_cells, A549_cells, 293T_cells 113936 W81552 Hs.83623 nuclear receptor subfamily 1; group I; m 2.43 293T_cells, OVCAR_cells, Fibroblasts 2 128862 R61297 Hs.106673 eukaryotic translation initiation factor 2.43 EB_cells, DU145_cells, DU145_cells 111614 R12581 Hs.191146 ESTs 2.43 HMEC (total RNA), Fibroblasts 2, MB-MDA-435s 111993 R42241 Hs.106359 ESTs 2.43 A549_cells, DU145_cells, CALU6_cells 131554 AA100026 Hs.28669 ESTs; Weakly similar to PROTEIN-TYROSINE 2.43 EB_cells, LNCaP_cells, Caco2 130983 N71215 Hs.21862 NCK-associated protein 1 2.42 EB_cells, Caco2, A549_cells 131654 AA497050 Hs.30204 ESTs 2.42 MCF7, MB-MDA-435s, Lu_SC_H345 105014 AA121123 Hs.191374 ESTs 2.42 EB_cells, Lu_AD_H23, Lu_LC_H460 106300 AA435840 Hs.19114 high-mobility group (nonhistone chromoso 2.42 EB_cells, LuSC_H345, A549_cells 102386 U40998 Hs.81728 unc119 (C.elegans) homolog 2.42 OVCAR_cells, EB_cells, DU145_cells 112517 R68589 Hs.23721 ESTs 2.42 Caco2, MCF7, DU145_cells 125375 H72971 KIAA0277 gene product 2.42 Lu_SC_H345, OVCAR_cells, Lu_SC_H69 123808 AA620552 Hs.25682 ESTs; Weakly similar to PHOSPHATIDYLETHA 2.42 EB_cells, Lu_AD_H23, Lu_SC_H69 114950 AA243503 Hs.11801 adenosine A2b receptor pseudogene 2.42 MB-MDA-453, HT29_cells, Lu_LC_H460 129906 H39216 Hs.239970 ESTs; Weakly similar to ZNF91L [H.sapien 2.41 Lu_SC_H345, Fibroblasts 2, DU145_cells 103408 X95876 Hs.198252 G protein-coupled receptor 9 2.41 RPWE_2, PRSC_log, Lu_SC_H345 129703 AA401348 Hs.179999 ESTs 2.41 EB_cells, 293T_cells, DU145_cells 105693 AA287104 Hs.181368 U5 snRNP-speciflc protein (220 kD); orth 2.41 293T_cells, CALU6_cells, A549_cells 106532 AA453628 Hs.37443 ESTs 2.41 ES_cells, OVCAR_cells, Caco2 132132 AA010933 Hs.4055 core promoter element binding protein 2.41 HMEC, HMEC (total RNA), EB_cells 111409 R00311 Hs.18798 EST; Weakly similar to !!!! ALU SUBFAMIL 2.41 Lu_SC_H345, Lu_SC_H69, PRSC_con 133813 M26657 Hs.250711 dipeptidyl carboxypeptidase 1 (angiotens 2.41 HT29_cells, BT474_cells, MB231_cells 127240 AA888387 Hs.243845 ESTs; Moderately similar to !!!! ALU SUB 2.41 Lu_SC_H345, DU145_cells, LNCaP_cells 104975 AA086071 Hs.50758 chromosome-associated polypeptide C 2.41 OVCAR_cells, DU145_cells, PC3_cells 118078 N54321 Hs.47790 EST 2.41 EB_cells, Fibroblasts 2, HMEC (total RNA) 115840 AA429253 Hs.58103 A kinase (PRKA) anchor protein 9 2.41 OVCAR_cells, EB_cells, PC3_cells 101186 L20298 Hs.179881 core-binding factor; beta subunit 2.4 EB_cells, DU145_cells, CALU6_cells 113098 T40936 Hs.8349 ESTs 2.4 Caco2, HT_cells, EB_cells 115185 AA259140 Hs.60238 ESTs 2.4 Lu_SC_H69, EB_cells, Caco2 113778 W15263 Hs.5422 ESTs 2.4 Caco2, MB-MDA-435s, LNCaP_cells 128261 AI061213 Hs.13179 ESTs; Moderately similar to !!!! ALU SUB 2.4 DU145_cells, LNCaP_cells, OVCAR_cells 132210 AA235013 Hs.42322 A kinase (PRKA) anchor protein 2 2.4 Caco2, DU145_cells, PRSC_log 112561 R72427 Hs.129873 ESTs; Weakly similar to CYTOCHROME P450 2.4 Lu_SQ_H520, Lu_AD_H23, EB_cells 127598 AA610677 Hs.168851 ESTs 2.4 LNCaP_cells, DU145_cells, OVCAR_cells 106664 AA460969 Hs.7510 mitogen-activated protein kinase kinase 2.4 OVCAR_cells, 293T_cells, A549_cells 131367 AA456687 Hs.26057 ESTs 2.4 EB_cells, MB-MDA-453, 293T_cells 103163 X67683 H.sapiens mRNA for keratin 4 2.39 EB_cells, LuAD_H23, Lu_AD_358 109639 F04444 Hs.6217 ESTs; Weakly similar to !!!! ALU SUSFAMI 2.39 EB_cells, Lu_SC_H345, Lu_SC_H69 112007 R42671 Hs.140853 EST; Weakly similar to !!!! ALU SUBFAMIL 2.39 MB-MDA-435s, Lu_SC_H345, Lu_AD_H23 100023 AFFX control: BioC-3 2.39 Caco2, Lu_AD_358, LNCaP_cells 119923 W86214 Hs.184642 ESTs 2.39 EB_cells, HS578T_cells, DU145_cells 127705 AJ003307 AJ003307 Selected dir 21 cDNA library H 2.39 Lu_AD_H23, Lu_SC_H345, Lu_LC_H460 130362 AA182658 Hs.179817 DKFZP586F0222 protein 2.39 EB_cells, DU145_cells, PC3_cells 100168 D14874 Hs.394 adrenomedullin 2.39 Fibroblasts 2, Caco2, HS578T_cells 134261 AA227678 Hs.8084 Human DNA seq from clone 465N24 on chr 1 2.39 PRSC_con, MB-MDA-453, LNCaP_cells Contains two novel genes; ESTs; GSSs an 103392 X94563 H.sapiens dbi/acbp gene exon 1 & 2 2.38 ES_cells, Lu_AD_H23, Lu_SC_H69 129888 U81001 Hs.131891 Human SNRPN mRNA; 3′ UTR; partial seq 2.38 LNCaP_cells, Lu_SC_H69, Lu_LC_H460 130119 T12649 Hs.251653 tubulin; beta; 2 2.38 Lu_AD_H23, Lu_LC_H460, Lu_LC_H460 118136 N57710 Hs.233952 proteasome (prosome; macropain) subunit 2.38 293T_cells, OVCAR_cells, HS578T_cells 131163 H80107 Hs.23754 ESTs 2.38 Lu_AD_H23, Lu_SC_H69, Lu_SC_H345 115964 AA448622 Hs.74313 ESTs 2.38 EB_cells, LNCaP_cells, DU145_cells 135026 H59730 Hs.93231 ESTs 2.37 EB_cells, 293T_cells, Lu_SC_H69 133300 D51401 Hs.70333 ESTs 2.37 OVCAR_cells, Caco2, CALU6_cells 129948 H69281 Hs.13643 ESTs 2.37 EB_cells, Lu_AD_H23, Lu_SC_H345 112505 R67923 Hs.23368 ESTs 2.37 DU145_cells, OVCAR_cells, 293T_cells 130715 T98227 Hs.171952 occludin 2.37 Caco2, LNCaP_cells, DU145_cells 120301 AA192163 Hs.104085 EST 2.37 Lu_AD_H23, EB_cells, PRSC_con 128062 AA379500 Hs.193155 ESTs 2.37 EB_cells, LNCaP_cells, DU145_cells 127154 AA789101 Hs.198860 ESTs; Weakly similar to !!!! ALU SUBFAMI 2.37 HS578T_cells, MCF7, Lu_SC_H69 102814 U90716 Hs.79187 coxsackie virus and adenovirus receptor 2.37 OVCAR_cells, DU145_cells, Lu_SC_H345 120239 Z41691 Hs.65919 ESTs 2.37 EB₁₃ cells, DU145_cells, LNCaP_cells 106829 AA481883 Hs.31236 ESTs; Weakly similar to Unknown [H.sapie 2.37 EB_cells, DU145_cells, OVCAR_cells 132681 AA435762 Hs.54894 ESTs; Highly similar to unknown [H.sapie 2.37 EB_cells, LNCaP_Cells, PRSC_con 108845 AA132946 Hs.68864 ESTs 2.36 Lu_AD_H23, Lu_AD_358, Lu_SQ_H520 133226 T85327 Hs.169552 ESTs 2.36 Caco2, MB-MDA-453, MCF7 106789 AA478726 Hs.26373 ESTs; Moderately similar to !!!! ALU SUB 2.36 MS-MDA-453, Caco2, OVCAR_cells 119236 T10166 Hs.237297 ESTs 2.36 EB_cells, 293T_cells, LNCaP_cells 106619 AA459255 Hs.23956 ESTs 2.36 LNCaP_cells, A549_cells, Caco2 109178 AA181600 Hs.62741 ESTs 2.36 Lu_SC_H345, LNCaP_cells, EB_cells 112724 R91753 Hs.17757 ESTs 2.36 Caco2, EB_cells, DU145_cells 112655 R85069 Hs.141139 ESTs 2.36 Fibroblasts 2, Lu_AD_H23, Lu_LC_H460 132820 AA454988 Hs.57621 ESTs 2.36 EB_cells, OVCAR_cells, HS578T_cells 106155 AA425309 Hs.33287 nuclear factor I/B 2.36 OVCAR_cells, Lu_SC_H345, MB-MDS-453 114632 AA084742 Hs.194380 ESTs; Weakly similar to !!!! ALU SUSFAMI 2.35 Lu_SC_H345, Lu_LC_H460, Lu_AD_H23 134776 J05582 Hs.89603 mucin 1; transmembrane 2.35 DU145_cells, Lu_AD_H23, Lu_AD_358 101192 L20859 Hs.78452 solute carrier family 20 (phosphate tran 2.35 PC3_cells, CALU6_cells, MS-MDA-435s 130349 W16686 Hs.171825 basic helix-loop-helix domain containing 2.35 A649_cells, DU145_cells, HT29_cells 106389 AA448949 Hs.6236 ESTs 2.36 LNCaP_cells, PC3_cells, DU145_cells 109637 F04426 Hs.23131 kinesin family member C3 2.35 MB-MDA-435s, A549_cells, Lu_LC_H460 101483 M24486 Hs.76768 procollagen-proline; 2-oxoglutarate 4-di 2.35 PC3_cells, HS578T_cells, EB_cells 131751 H18335 Hs.31562 ESTs 2.35 DU145_cells, MB231_cells, HMEC 131050 X13967 Hs.2250 leukemia inhibitory factor (cholinergic 2.35 Lu_AD_H23, PC3_cells, PRSC_log 130097 N21159 Hs.14845 forkhead box O3A 2.34 EB_cells, LNCaP_cells, LNCaP_cells 134533 AA013468 Hs.241493 natural killer-tumor recognition seq 2.34 EB_cells, HT29_cells, HMEC 134839 D63479 Hs.115907 diacylglycerol kinase; delta (130 kD) 2.34 Lu_LC_H460, Caco2, DU145_cells 115690 AA410894 Hs.44159 ESTs 2.34 PC3_cells, EB_cells, OVCAR_cells 129079 N91011 Hs.108502 ESTs 2.34 Lu_AD_H23, Lu_SC_H69, Lu_AD_358 123517 AA608525 Hs.243059 EST 2.34 Lu_SC_H345, PC3_cells, MS-MDA-435s 126239 AA527215 Hs.75879 ribosomal protein L19 2.34 BT474_cells, Lu_LC_H460, Lu_AD_H23 124440 N46435 ESTs 2.34 Lu_SC_H69, HT29_cells, MS-MDA-435s 111468 R05809 Hs.205481 ESTs 2.34 Lu_AD_H23, PRSC_log, Lu_SQ_H520 129560 H18428 Hs.113613 ESTs; Moderately similar to !!!! ALU SUB 2.34 Lu_SC_H69, Lu_SC_H345, LNCaP_cells 104857 AA043219 Hs.19058 ESTs 2.34 Lu_AD_H23, Lu_SC_H345, Lu_SC_H345 109647 F04587 Hs.28241 ESTs 2.34 HS578T_cells, A549_cells, CALU6_cells 117160 H97817 Hs.183302 ESTs 2.34 EB_cells, Fibroblasts 2, Lu_SC_H69 112352 R58974 Hs.167343 ESTs 2.34 EB_cells, Lu_SC_H345, HT29_cells 113653 T95745 Hs.187433 ESTs 2.34 MB-MDA-435s, MB-MDA-453, Lu_SC_H345 131606 W56804 Hs.29385 AFG3 (ATPase family gene 3; yeast)-like 2.34 OVCAR_cells, Fibroblasts 2, MB-MDA-435s 101525 M29536 Hs.12163 eukaryotic translation initiation factor 2.34 EB_cells, Caco2, DU145_cells 125921 AA775029 Hs.122591 ESTs 2.33 293T_cells, PRSC_log, Lu_SC_H345 125775 AA213555 Hs.29205 alpha integrin binding protein 63 2.33 EB_cells, DU145_cells, LNCaP_cells 108743 AA126917 Hs.71074 ESTs 2.33 Lu_AD_H23, Lu_AD_358, Lu_LC_H460 133735 AC002045 Hs.251928 nuclear pore complex interacting protein 2.33 LNCaP_cells, Lu_SC_H69, DU145_cells 120403 AA234916 Hs.243851 ESTs 2.33 MB231_cells, Lu_SC_H345, Lu_SC_H69 134998 R02207 Hs.92679 ESTs; Weakly similar to microtubule-base 2.33 LNCaP_cells, BT474_cells, MCF7 108456 AA079326 Hs.143654 ESTs 2.33 HT29_cells, Lu_AD_H23, RPWE_2 130552 M86667 Hs.179662 nucleosome assembly protein 1-like 1 2.33 EB_cells, A549_cells, DU145_cells 111114 N63391 Hs.9238 ESTs 2.33 Caco2, EB_cells, MB-MDA-453 127767 AI269498 Hs.125543 ESTs; Moderately similar to TADA1 protei 2.33 CALU6_cells, 293T_cells, PC3_cells 106546 AA454725 Hs.21056 H sapiens mRNA from chromosome 5q21-22; 2.33 OVCAR_cells, Caco2, LNCaP_cells 122379 AA446110 Hs.250989 EST 2.33 BT474_cells, Fibroblasts 2, MB-MDA-435s 133650 D84294 Hs.118174 tetratricopeptide repeat domain 3 2.33 Lu_SC_H345, EB_cells, EB_cells 106434 AA449099 Hs.8151 ESTs; Weakly similar to atopy related au 2.33 EB_cells, LNCaP_cells, Caco2 105297 AA233451 Hs.183858 transcriptional intermediary factor 1 2.33 EB_cells, LNCaP_cells, Caco2 115976 AA447442 Hs.86327 ESTs 2.33 EB_cells, 293T_cells, Lu_SC_H69 105788 AA351031 Hs.23965 solute carrier family 22 (organic anion 2.33 EB_cells, Lu_AD_H23, Lu_SC_H345 113774 W04550 Hs.9927 H sapiens mRNA; cDNA DKFZp564D156 (from 2.32 OVCAR_cells, EB_cells, Lu_SC_H69 110617 H68772 Hs.35820 ESTs; Weakly similar to b3418.1 [H.sapie 2.32 Lu_SC_H345, Lu_AD_H23, PRSC_con 102234 U26312 Hs.8123 chromobox homolog 3 (Drosophila HP1 gamm 2.32 CALU6_cells, LNCaP_cells, A549_cells 114777 AA151699 Hs.184519 ESTs; Weakly similar to !!!! ALU SUBFAMI 2.32 HT29_cells, Fibroblasts 2, Lc_SC_H345 125518 R20148 Hs.193851 ESTs 2.32 HT29_cells, HMEC (total RNA), MB231_cells 130814 AA256695 Hs.19813 ESTs 2.32 MB-MDA-435s, Lu_SC_H69, PRSC_log 123473 AA599143 ESTs; Moderately similar to !!!! ALU SUB 2.32 LNCaP_cells, DU145_cells, Lu_H345 134310 AA313414 Hs.8148 H sapiens clone 24856 mRNA seq; complete 2.32 PC3_cells, LNCaP_cells, OVCAR_cells 119192 R85375 Hs.237262 EST 2.32 Lu_SC_H69, PRSC_log, PRSC_con 114391 AA004876 Hs.133100 ESTs 2.32 PC3_cells, 293T_cells, 293T_cells 119133 R49144 Hs.119756 ESTs 2.32 PRSC_log, 293T_cells, 293T_cells 109710 F09792 Hs.12929 ESTs 2.32 Lu_AD_H23, Lu_SC_H69, Lu_SC_H345 116726 F13681 Hs.42309 ESTs 2.32 MCF7, BT474_cells, MB-MDA-453 133206 R32993 Hs.6762 ESTs; Weakly similar to similar to leucy 2.31 DU145_cells, 293T_cells, EB_cells 135163 AA125988 Hs.199955 ESTs 2.31 Lu_SC_H345, LNCaP_cells, DU145_cells 111219 N68836 Hs.19247 ESTs 2.31 OVCAR_cells, LNCaP_cells, 293T_cells 110283 H29565 Hs.12271 ESTs 2.31 BT474_cells, MB231_cells, MB231_cells, MB-MDA-453 103772 AA092473 Hs.8123 chromobox homolog 3 (Drosophila HP1 gamm 2.31 CALU6_cells, MCF7, DU145_cells 122766 AA459386 Hs.194058 ESTs; Weakly similar to atypical PKC spe 2.31 HT_cells, BT474_cells, HMEC 120886 AA365566 Hs.132736 ESTs; Weakly similarto allograft inflam 2.31 DU145_cells, A549_cells, Lu_LC_H460 123512 AA600248 Hs.142245 HERV-H LTR-associating 3 2.31 PC3_cells, 293T_cells, DU145_cells 106644 AA460239 Hs.12680 ESTs 2.31 HS578T_cells, MB231_cells, Lu_SQ_H520 127359 H72971 KIAA0277 gene product 2.31 Lu_SC_H345, DU145_cells, OVCAR_cells 105919 AA402494 Hs.3990 ESTs 2.31 HS578T_cells, DU145_cells, LNCaP_cells 125241 W86291 Hs.121593 ESTs 2.3 HMEC, HMEC (total RNA), EB_cells 104624 AA001936 Hs.184721 ESTs 2.3 DU145_cells, PC3_cells, PRSC_log 128765 AA101767 Hs.10494 ESTs 2.3 EB_cells, HMEC (total RNA), Lu_LC_H460 108360 AA071539 zm74b6.s1 Stratagene neuroepithelium (#9 2.3 HT29_cells, RPWE_2, Lu_AD_H23 HYDROXYSTEROID DEHYDROGENASEIDELTA-5-DEL 115682 AA410300 Hs.44618 ESTs 2.3 HT29_cells, Lu_SQ_H520, Lu_AD_H23 134528 M23161 Hs.84775 Human transposon-like element mRNA 2.3 EB_cells, CALU6_cells, A549_cells 111091 N59858 Hs.33032 H sapiens mRNA; cDNA DKFZp434N185 (from 2.3 LNCaP_cells, DU145_cells, PRSC_log 134044 AA262475 Hs.78746 phosphodiesterase 8A 2.29 DU145_cells, A549_cells, MCF7 118229 N62339 Hs.180532 heat shock 90 kD protein 1; alpha 2.29 MCF7, DU145_cells, EB_cells 110188 H20522 Hs.20969 ESTs 2.29 Fibroblasts 2, MB-MDA-435s, Lu_LC_H460 125073 T87185 Hs.193638 ESTs; Weakly similar to !!!! ALU CLASS C 2.29 EB_cells, Lu_SC_H345, Lu_SC_H69 111495 R07210 Hs.19913 ESTs 2.29 CALU6_cells, EB_cells, MCF7 124024 F03077 Hs.106672 ESTs 2.29 HS578T_cells, RPWE_2, Lu_AD_358 128230 AA984074 Hs.176757 ESTs 2.29 LNCaP_cells, DU145_cells, OVCAR_cells 125471 AA477571 Hs.152601 UDP-glucose ceramide glucosyltransferase 2.29 DU145_cells, PRSC_con, PRSC_log 120734 AA299949 EST12545 Uterus tumor I H sapiens cDNA 3 2.28 Lu_AD_H23, Lu_SC_H345, Lu_SC_H69 134349 AA406373 Hs.8208 ESTs 2.28 DU145_cells, PC3_cells, LNCaP_cells 123412 AA521443 Hs.187763 ESTs 2.28 BT474_cells, BT474_cells, Lu_SC_H169 116297 AA489042 Hs.59498 ESTs 2.28 EB_cells, 293T_cells, MB-MDA-453 104476 N33807 Hs.223014 protease; serine; 15 2.28 LNCaP_cells, MCF7, PC3_cells 101004 J04101 Hs.248109 v-ets avian erythroblastosis virus E26 o 2.28 HT29_cells, MB-MDA-435s, HMEC (total RNA) 109991 H09813 Hs.12896 KIAA1034 protein 2.28 EB_cells, CALU6_cells, 293T_cells 118934 N92571 Hs.54808 ESTs 2.28 HS578T_cells, 293T_cells, A549_cells 125096 T94328 Hs.194533 ESTs 2.28 Lu_SC_H345, Lu_SC_H69, 293T_cells 117514 N32226 Hs.124058 ESTs 2.28 CALU6_cells, HMEC, Lu_AD_H23 132792 AA401903 Hs.242985 hemoglobin; gamma G 2.28 OVCAR_cells, Lu_SC_H69, MCF7 129009 AA131421 Hs.107884 ESTs 2.28 Hs578T_cells, CALU6_cells, Caco2 111658 R16981 Hs.15276 ESTs 2.28 MB-MDA-435s, 293T_cells, A549_cells 112322 R55757 Hs.26457 EST 2.28 Lu_SC_H345, Lu_SC_H69, Lu_AD_358 133477 W69310 Hs.740 PTK2 protein tyrosine kinase 2 2.28 EB_cells, PC3_cells, DU145_cells 132149 T10822 Hs.4095 ESTs 2.28 LNCaP_cells, EB_cells, PC3_cells 115119 AA256524 Hs.46847 Human DNA seq from done 30M3 on chromos 2.27 A549_cells, EB_cells, LNCaP_cells yeast and archaea bacterial genes; and 102130 U15009 Hs.1575 small nuclear ribonucleoprotein D3 polyp 2.27 LNCaP_cells, Caco2, EB_cells 114343 Z41424 Hs.21259 ESTs 2.27 HT29_cells, OVCAR_cells, Fibroblasts 2 106746 AA476436 Hs.7991 ESTs 2.27 Lu_AD_358, RPWE_2, Lu_AD_H23 119359 T71021 Hs.93334 ESTs; Highly similar to WS basic-helix-I 2.27 Lu_SC_H69, 293T_cells, DU145_cells 106301 AA435867 Hs.168212 kinesin family member 3B 2.27 OVCAR_cells, LNCaP_cells, EB_cells 130280 L13738 Hs.153937 activated p21cdc42Hs kinase 2.27 MB-MDA-453, DU145_cells, DU145_cells 119724 W69468 Hs.47622 ESTs 2.27 PC3_cells, HT29_cells, A549_cells 108960 AA150199 Hs.49378 DKFZP586D0919 protein 2.27 EB_cells, HS578T_cells, Lu_AD_358 103489 Y08614 Hs.79090 exportin 1 (CRM1; yeast; homolog) 2.26 EB_cells, CALU6_cells, DU145_cells 107711 AA015736 Hs.220687 ESTs 2.26 EB_cells, Lu_AD_H23, Lu_AD_358 131950 W84704 Hs.35380 ESTs 2.26 HS578T_cells, OVCAR_cells, MB-MDA-435s 107093 AA609600 Hs.10018 ESTs 2.26 LNCaP_cells, OVCAR_cells, DU145_cells 113649 T95641 Hs.16400 ESTs; Weakly similar to Hrs [H.sapiens] 2.26 Lu_AD_H23, Lu_SC_H69, PRSC_log 105255 AA227498 Hs.3623 ESTs 2.26 HS578T_cells, 293T_cells, Lu_SC_H345 130094 H43286 Hs.167017 gamma-aminobutyric acid (GABA) B recepto 2.26 Fibroblasts 2, MB231_cells, 293T_cells 111874 R37959 Hs.13358 ESTs 2.26 CALU6_cells, Lu_SQ_H520, 293T_cells 107890 AA026030 Hs.61311 ESTs; Weakly similar to CALPAIN 2; LARGE 2.26 HT29_cells, MB-MDA-453, PC3_cells 124628 N74702 Hs.102834 ESTs 2.26 293T_cells, CALU6_cells, CALU6_cells 119707 W67569 Hs.44143 ESTs; Weakly similar to SNF2alpha protei 2.26 293T_cells, OVCAR_cells, Lu_SC_H345 106737 AA470080 Hs.36237 ESTs; Moderately similar to CGI-34 prote 2.26 LNCaP_cells, DU145_cells, MB-MDA-435s 117305 N22798 Hs.43248 EST 2.26 HT29_cells, BT474_cells, Fibroblasts 2 134470 X54942 Hs.83758 CDC28 protein kinase 2 2.26 DU145_cells, CALU6_cells, LNCaP_cells 130734 T99337 Hs.18624 KIAA1052 protein 2.26 Lu_AD_H23, Lu_SC_H345, Lu_SC_H69 128561 R69227 Hs.101489 ESTs 2.26 Lu_SC_H345, DU145_cells, OVCAR_cells 100670 HG2992-H Beta-Hexosaminidase, Alpha Polypeptide, 2.26 HT29_cells, BT474_cells, Lu_SC_H345 115953 AA443958 Hs.90960 ESTs 2.26 Caco2, 293T_cells, DU145_cells 129612 H17476 Hs.11615 ESTs; Highly similarto map kinase phosp 2.25 CALU6_cells, LNCaP_cells, PC3_cells 111362 N91973 Hs.23595 deoxyribonuclease III; dnaQ/mutD (E. col 2.25 Lu_SQ_H520, Lu_AD_H23, RPWE_2 116275 AA485453 Hs.250911 interleukin 13 receptor; alpha 1 2.25 OVCAR_cells, 293T_cells, DU145_cells 114461 AA024848 Hs.126705 ESTs 2.25 EB_cells, Lu_AD_H23, Lu_AD_H23 134083 AA278393 Hs.79013 ESTs 2.25 293T_cells, EB_cells, OVCAR_cells 132470 Z24724 Hs.4934 H.sapiens polyA site DNA 2.25 EB_cells, HS578T_cells, Caco2 114718 AA131328 zo8d1.s1 Stratagene neuroepithelium NT2R 2.25 MB-MDA-435s, HT29_cells, Lu_SC_H69 SW:COX2_MOUSE P45 CYTOCHROME C OXIDASE P 129499 R40395 Hs.242908 lecithin-cholesterol acyltransferase 2.25 HMEC (total RNA), Fibroblasts 2, HMEC 124758 R38422 Hs.169168 ESTs 2.25 293T_cells, RPWE_2, Lu_LC_H460 130301 X83127 Hs.172471 potassium voltage-gated channel; shaker- 2.25 EB_cells, OVCAR_cells, A549_cells 131263 R38334 Hs.24950 regulator of G-protein signalling 5 2.25 Lu_AD_H23, EB_cells, Lu_SC_H69 107159 AA621340 Hs.10600 ESTs; Weakly similarto ORF YKR081c [S.c 2.25 LNCaP_cells, HMEC, EB_cells 133262 N72009 Hs.206710 ESTs 2.24 Lu_SC_H345, DU145_cells, LNCaP_cells 132985 AA093619 Hs.62113 KIAA0717 protein 2.24 EB_cells, Lu_AD_H23, Lu_AD_358 114172 Z39043 Hs.21421 ESTs; Weakly similar to cysteine desulfu 2.24 293T_cells, CALU6_cells, Lu_SQ_H520 127847 AA913387 Hs.126717 ESTs 2.24 LNCaP_cells, DU145_cells, Lu_SC_H69 106499 AA452244 Hs.16727 ESTs 2.24 Lu_SC_H345, MB-MDA-453, Lu_SC_H69 105095 AA150088 Hs.27023 KIAA0917 protein 2.24 DU145_cells, LNCaP_cells, CALU6_cells 108876 AA134361 Hs.191453 ESTs 2.24 EB_cells, Lu_SC_H345, Lu_AD_H23 121971 AA429667 Hs.120405 ESTs 2.24 Lu_AD_H23, 293T_cells, CALU6_cells 114334 Z41342 Hs.22941 ESTs 2.24 DU145_cells, PC3_cells, EB_cells 114565 AA063001 Hs.103527 SH2 domain protein 2A 2.24 Lu_LC_H460, MCF7, HMEC (total RNA) 115766 AA421761 Hs.77603 ESTs 2.24 Fibroblasts 2, MB-MDA-435s, MB231_cells 130989 AA608546 Hs.21906 ESTs 2.24 PC3_cells, LNCaP_cells, DU145_cells 116304 AA489461 Hs.64742 H sapiens mRNA for KIAA0540 protein; par 2.24 BT474_cells, EB₁₃ cells, LNCaP_cells 111154 N66545 Hs.29169 ESTs 2.24 OVCAR_cells, MB-MDA-435s, HMEC 105561 AA262881 Hs.16029 ESTs; Weakly similar to altematively sp 2.23 HS578T_cells, A549_cells, HMEC 105939 AA404421 Hs.12258 ESTs 2.23 EB₁₃ cells, LNCaP_cells, DU145_cells 126379 AI085342 Hs.166146 Homer; neuronal immediate earty gene; 3 2.23 HS578T_cells, PC3_cells, RPWE_2 106610 AA458882 Hs.4832 ESTs; Moderately similar to Lasp-1 prote 2.23 DU145_cells, MCF7, Lu_SC_H345 132786 AA424545 Hs.56851 H sapiens mRNA expressed in placenta 2.23 EB_cells, Lu_AD_H23, Fibroblasts 2 107206 D20728 Hs.30767 ESTs 2.23 BT474_cells, Fibroblasts 2, MB-MDA-435s 133708 R42172 Hs.75667 synaptophysin 2.23 Lu_SC_H345, CALU6_cells, Lu_SC_H69 135123 AA227567 Hs.9482 target of myb 1 (chicken) homolog 2.23 BT474_cells, MB231_cells, EB_cells 132156 AA157401 Hs.4113 S-adenosylhomocysteine hydrolase-like 1 2.23 DU145_cells, 293T_cells, LNCaP_cells 116934 H75624 Hs.39662 ESTs 2.23 CALU6_cells, Lu_SC_H345, Lu_LC_H460 133660 R87373 ym88e05.r1 Soares aduh brain N2b4HB55Y 2.23 DU145_cells, A549_cells, PC3_cells IMAGE: 166016 5′, mRNA seq. 119458 W23633 Hs.125043 ESTs 2.23 293T_cells, MB-MDA-453, OVCAR_cells 101247 L33801 Hs.78802 glycogen synthase kinase 3 beta 2.23 LNCaP_cells, EB_cells, MB-MDA-435s 126008 AA253460 zs06f04.s1 NCI_CGAP_GCB1 H sapiens cDNA 2.23 HT29_cells, PRSC_log, Fibroblasts 2 122938 AA477119 zu37c7.s1 Soares ovary tumor NbHOT H sap 2.23 PC3_cells, MCF7, MB-MDA-434s TR: G288289 G288289 MITOCHONDRIAL D-LOOP 114148 Z38804 Hs.184777 ESTs; Moderately similar to OPIOID BINDI 2.23 HS578T_cells, Fibroblasts 2, LuSC_H345 MOLECULE PRECURSOR [H.sapiens] 103433 X98001 Hs.78948 Rab geranylgeranyltransferase; beta subu 2.22 LNCaP_cells, EB_cells, 293T_cells 132954 AA027112 Hs.216194 ESTs 2.22 EB_cells, Lu_AD_H23, Fibroblasts 2 133228 N90029 Hs.6831 H sapiens clone 1400 unknown protein mRN 2.22 293T_cells, PC3_cells, DU145_cells 103891 AA242887 Hs.124186 ring finger protein 2 2.22 EB_cells, Lu_SC_H69, Lu_SC_H345 124883 R75630 Hs.177242 ESTs 2.22 EB_cells, Lu_AD_H23, Lu_SC_H345 109921 H05734 Hs.30559 ESTs 2.22 Lu_SQ_H520, 293T_cells, RPWE_2 127306 AI305162 Hs.193687 ESTs 2.22 MCF7, HT29_cells, MB-MDA-453 102707 U77456 Hs.78103 nucleosome assembly protein 1-like 4 2.22 Caco2, EB_cells, CALU6_cells 106193 AA427625 Hs.23272 ESTs 2.22 293T_cells, EB_cells, A549_cells 118819 N79045 Hs.50800 ESTs; Weakly similar to !!!! ALU SUBEAMI 2.22 Lu_SC_H345, LuSC_H69, DU145_cells 134326 U16306 Hs.81800 chondroitin sulfate proteoglycan 2 (vers 2.22 HS578T_cells, PRSC_log, CALU6_cells 112241 R51248 Hs.16027 ESTs 2.22 293T_cells, HMEC (total RNA), HMEC (total RNA) 123693 AA609591 Hs.112728 ESTs 2.22 HT29_cells, HMEC (total RNA), BT474_cells 129052 AA496297 Hs.182740 ribosomal protein S11 2.22 EB_cells, Lu_AD_H23, Lu_AD_358 122481 AA448271 Hs.99126 ESTs 2.21 Lu_AD_H23, HT29_cells, Lu_AD_358 128895 R37753 Hs.106985 ESTs 2.21 EB_cells, Lu_AD_H23, Lu_SC_H345 124691 R05835 Hs.110153 ESTs; Weakly similar to B-CELL GROWTH FA 2.21 EB_cells, Lu_AD_H23, Lu_AD_358 131556 AA442853 Hs.2869 cyclin-dependent kinase 5; regulatory su 2.21 HT29_cells, Lu_LC_H460, Lu_SC_H69 128869 AA424570 Hs.106736 ESTs 2.21 EB_cells, Lu_AD_H23, Lu_SC_H69 107114 AA610089 Hs.11776 U4/U6-associated RNA splicing factor 2.21 MCF7, Lu_SC_H345, DU145_cells 106255 AA431191 Hs.161489 ESTs 2.21 EB_cells, Caco2, DU145_cells 130724 AA370091 Hs.179680 ESTs 2.2 EB_cells, Lu_AD_H23, Lu_SC_H69 105483 AA255874 Hs.23458 ESTs 2.2 LNCaP_cells, DU145_cells, PC3_cells 118970 N93503 Hs.54961 stoned B/TFIIA-alpha/beta like factor 2.2 293T_cells, HS578T_cells, OVCAR_cells 120805 AA346041 Hs.96844 ESTs 2.2 HT29_cells, HS578T_cells, 293T_cells 106158 AA425382 Hs.6553 ESTs 2.2 CALU6_cells, PC3_cells, EB_cells 102121 U14391 Hs.82251 myosin IC 2.2 A549_cells, EB_cells, Caco2 109446 AA232125 Hs.87062 ESTs 2.2 HT29_cells, Lu_LC_H460, CALU6_cells 129515 AA490882 Hs.112227 ESTs 2.2 Lu_SC_H345, BT474_cells, Caco2 113128 T49325 Hs.8977 ESTs 2.2 Lu_SQ_H520, Lu_AD_H23, Lu_AD_358 127289 AI041014 Hs.220752 ESTs 2.2 EB_cells, Lu_AD_H23, Lu_AD_H23 129912 AA047344 Hs.107213 ESTs; Highly similar to NY-REN-6 antigen 2.2 CALU6_cells, A549_cells, EB_cells 115700 AA411655 Hs.67709 ESTs 2.2 OVCAR_cells, EB_cells, Caco2 106267 AA431873 Hs.4988 H sapiens clone 24711 mRNA seq 2.2 Lu_SQ_H520, EB_cells, PC3_cells 112881 T03593 Hs.182814 ESTs 2.19 A549_cells, OVCAR_cells, 293T_cells 116902 H70739 yu69f11.s1 Weizmann Olfactory Epithelium 2.19 LNCaP_cells, DU145_cells, PC3_cells IMAGE: 239085 3′ similar to contains LTR 105621 AA280865 Hs.6375 H sapiens mRNA; cDNA DKFZp564K0222 (from 2.19 HMEC, Caco2, HMEC (total RNA) 126991 R31652 Hs.821 biglycan 2.19 Fibroblasts 2, LuSC_H69, HS578T_cells 125466 R08234 Hs.180461 ESTs 2.19 Lu_AD_358, Lu_AD_H23, Lu_SQ_H520 108491 AA082973 zn7g1.s1 Stratagene hNT neuron (#937233) 2.19 Lu_AD_358, RPWE_2, Lu_LC_H460 to gb:M3672 6S RIBOSOMAL PROTEIN L7A (H 109978 H09356 Hs.22528 ESTs 2.19 PRSC_log, Lu_SC_H345, Lu_SC_H69 106990 AA521354 Hs.24758 ESTs 2.19 EB_cells, LNCaP_cells, OVCAR_cells 122362 AA443919 Hs.96840 ESTs 2.19 EB_cells, Lu_AD_358, PRSC_con 125367 AI016490 Hs.81964 SEC24 (S. cerevisiae) related gene famil 2.19 HT29_cells, Lu_SC_H69, Lu_AD_H23 110716 H97188 Hs.35096 ESTs 2.19 DU145_cells, Fibroblasts 2, PRSC_con 129297 R11267 Hs.180570 H sapiens chromosome 19; cosmid F22329 2.19 293T_cells, MB-MDA-435s, A549_cells 104992 AA102652 Hs.22753 ESTs; Weakly similar to coded for by C. 2.18 MCF7, MB-MDA-453, Lu_SQ_H520 119896 W84738 Hs.137319 ESTs 2.18 293T_cells, 293T_cells, OVCAR_cells 118594 N69022 Hs.49599 ESTs 2.18 Lu_SC_H69, Lu_AD_H23, Lu_SC_H345 129786 H98977 Hs.246109 ESTs 2.18 293T_cells, 293T_cells, 293T_cells 104325 D81608 Hs.150675 polymerase (RNA) II (DNA directed) polyp 2.18 PC3_cells, Lu_SC_H345, LNCaP_cells 123022 AA480909 aa28f10.s1 NCI_CGAP_GCB1 H sapiens cDNA 2.18 OVCAR_cells, DU145_cells, LNCaP_cells Alu repetitive element; contains element 133572 W94333 Hs.7499 translocase of inner mitochondrial membr 2.18 Caco2, LNCaP_cells, Lu_SQ_H520 133363 AA479713 Hs.71962 ESTs 2.18 EB_cells, Lu_AD_H23, Fibroblasts 2 135361 AA053319 Hs.167700 ESTs 2.18 EB_cells, 293T_cells, Caco2 128319 AA808904 Hs.115095 ESTs; Weakly similar to RHO-RELATED GTP- 2.18 Lu_SC_H345, OVCAR_cells, DU145_cells 128660 AA011597 Hs.177398 ESTs 2.18 EB_cells, Lu_AD_H23, Lu_SQ_H520 114877 AA235618 Hs.205125 ESTs 2.18 DU145_cells, 293T_cells, OVCAR_cells 125925 H28737 ESTs; Moderately similar to !!!! ALU SUB 2.18 Lu_SC_H69, Lu_SC_H345, HS578T_cells 113427 T85105 Hs.15471 ESTs 2.18 EB_cells, Lu_AD_H23, Lu_SC_H69 117500 N31909 Hs.44278 ESTs 2.18 PRSC_con, Lu_SC_H345, PRSC_log 131384 F13608 Hs.26226 ESTs 2.18 293T_cells, LNCaP_cells, OVCAR_cells 134499 U70370 Hs.84136 paired-like homeodomain transcnption fa 2.18 Caco2, BT474_cells, MB231_cells 128154 AA922969 Hs.127100 ESTs 2.17 MB-MDA-453, MB-MDA-453, Lu_SC_H345 134585 T48154 Hs.168655 H sapiens mRNA for H-2K binding factor-2 2.17 LNCaP_cells, 293T_cells, PRSC_log 104987 AA101723 Hs.16683 ESTs 2.17 EB_cells, MCF7, DU145_cells 132992 AA091017 Hs.6226 ESTs 2.17 Caco2, LNCaP_cells, DU145_cells 135311 M36089 Hs.98493 X-ray repair complementing defective rep 2.17 HMEC (total RNA), Fibroblasts 2, HMEC 113171 T54613 Hs.9761 EST 2.17 HT29_cells, PRSC_con, Lu_SQ_H520 117736 N46999 Hs.46648 ESTs 2.16 PRSC_log, OVCAR_cells, A549_cells 125181 W58461 Hs.12396 ESTs 2.16 LNCaP_cells, DU145_cells, 293T_cells 120187 Z40251 Hs.56974 ESTs 2.16 LNCaP_cells, MB-MDA-453, HMEC (total RNA) 100308 D50532 Hs.54403 macrophage lectin 2 (calcium dependent) 2.16 HT29_cells, Lu_AD_H23, Lu_AD_H23 110960 N50887 Hs.26549 ESTs; Weakly similar to KIAA0449 protein 2.16 Caco2, A549_cells, LNCaP_cells 113608 T93113 ESTs; Moderately similar to !!!! ALU SUB 2.16 Lu_SC_H69, CALU6_cells, 293T_cells 107538 Z21089 Hs.50094 ESTs; Weakly similar to KALIRIN [R.norve 2.16 HS578T_cells, 293T_cells, DU145_cells 128703 S76992 Hs.104005 vav 2 oncogene 2.16 RPWE_2, Lu_SC_H69, HT29_cells 126065 AI366484 ESTs 2.16 293T_cells, CALU6_cells, A549_cells 130000 AA465727 Hs.124084 ESTs; Weakly similar to !!!! ALU SUBFAMI 2.16 DU145_cells, LNCaP_cells, OVCAR_cells 120407 AA235040 Hs.107283 ESTs 2.16 EB_cells, 293T_cells, A549_cells 121199 AA400371 Hs.97792 ESTs 2.16 Lu_AD_358, Lu_AD_H23, A549_cells 114963 AA243867 Hs.193055 ESTs 2.16 DU145_cells, PRSC_con, LNCaP_cells 100343 D63874 Hs.189509 high-mobility group (nonhistone chromoso 2.15 CALU6_cells, MB-MDA-453, Caco2 125077 T88822 yd32f5.s1 Soares fetal liver spleen 1NFL 2.15 Lu_AD_H23, Lu_SC_H69, Lu_SC_H345 117286 N22181 yw36d12.s1 Morton Fetal Cochlea H sapien 2.15 293T_cells, Lu_Sc_H345, Lu_SC_H69 132876 AA130603 Hs.169683 ESTs; Moderately similarto !!!! ALU SUB 2.15 EB_cells, LNCaP_cells, HS578T_cells 133834 AA147510 Hs.154737 serine protease; umbilical endothelium 2.15 DU145_cells, EB_cells, Caco2 126908 AA169866 ESTs; Weakly similar to !!!! ALU SUBFAMI 2.15 DU145_cells, LNCaP_cells, OVCAR_cells 106900 AA490142 Hs.6193 ESTs 2.15 Fibroblasts 2, Lu_AD_H23, PRSC_con 129398 AA437374 Hs.234573 H sapiens mRNA for TL132 2.15 MCF7, DU145_cells, LNCaP_cells 114512 AA044274 Hs.165215 ESTs 2.15 Lu_AD_358, MB-MDA-453, HS578T_cells 134381 U56637 Hs.184270 capping protein (actin filament) muscle 2.15 LNCaP_cells, EB_cells, PC3_cells 118843 N80671 Hs.220255 ESTs 2.14 EB_cells, DU145_cells, MCF7 115526 AA342049 Hs.69606 ESTs 2.14 293T_cells, Caco2, Lu_SC_H69 123460 AA598981 Hs.251122 EST 2.14 Lu_SC_H345, DU145_cells, MCF7 119812 W73951 Hs.58348 ESTs; Weakly similar to CORNIFIN A [H.sa 2.14 293T_cells, HS578T_cells, CALU6_cells 105263 AA227926 Hs.6682 ESTs 2.14 A549_cells, HMEC (total RNA), EB_cells 129242 W81679 Hs.5174 ribosomal protein S17 2.14 293T_cells, CALU6_cells, HMEC (total RNA) 132348 AA037285 Hs.170311 heterogeneous nuclear ribonucleoprotein 2.14 A549_cells, HT29_cells, Lu_SQ_H520 114425 AA015763 Hs.132812 ESTs 2.14 293T_cells, HS578T_cells, PRSC_con 127759 AI369384 arylsulfatase D 2.14 DU145_cells, LNCaP_cells, EB_cells 134069 U29607 Hs.78935 methionine aminopeplidase; elF-2-associa 2.14 Lu_SC_H345, DU145_cells, MCF7 116158 AA461187 Hs.61762 ESTs 2.14 Lu_SC_H69, MCF7, MB-MDA-453 125627 R35166 Hs.14881 ESTs 2.14 HT29_cells, Fibroblasts 2, BT474_cells 118684 N71364 Hs.109510 ESTs 2.14 OVCAR_cells, PRSC_con, HS578T_cells 119419 T97977 Hs.60260 ESTs 2.14 Lu_AD_H23, Lu_SQ_H520, Lu_SQ_H520 133097 N67515 Hs.6479 ESTs; Weakly similar to KIAA0872 protein 2.14 EB_cells, Lu_AD_H23, Lu_AD_358 112121 R45445 Hs.252723 H sapiens mRNA; cDNA DKFZp434D115 (from 2.13 Lu_AD_H23, Lu_AD_358, BT474_cells 114894 AA236019 Hs.188803 ESTs 2.13 MB-MDA-453, MCF7, Lu_SQ_H520 124087 H08773 y194d5.s1 Soares infant brain 1NIB H sap 2.13 Lu_SC_H69, Fibroblasts 2, HMEC (total RNA) 111902 R39191 Hs.109445 KIAA1020 protein 2.13 Caco2, 293T_cells, Lu_SC_H69 119943 W86835 Hs.14158 copine III 2.13 LNCaP_cells, PC3_cells, HS578T_cells 109276 AA196306 Hs.86045 ESTs 2.13 Lu_SC_H345, Lu_SC_H69, Lu_LC_H460 117351 N24581 Hs.43230 ESTs 2.13 HS578T_cells, CALU6_cells, PRSC_con 116046 AA453461 Hs.94491 H sapiens clone 23585 mRNA seq 2.13 LNCaP_cells, Caco2, EB_cells 112785 R96478 Hs.16586 ESTs 2.13 EB₁₃ cells, Lu_AD_H23, Lu_SC_H69 115835 AA428576 Hs.41371 ESTs 2.13 EB_cells, Lu_SC_H345, OVCAR_cells 127499 T49891 Hs.119252 tumor protein; translationally-controlle 2.13 EB_cells, PRSC_con, LNCaP_cells 129951 AA019475 Hs.74615 platelet-derived growth factor receptor, 2.13 EB_cells, Lu_AD_H23, Lu_SC_H69 124270 H79560 Hs.107840 ESTs 2.13 OVCAR_cells, 293T_cells, 293T_cells 133766 D52420 Hs.184326 cell division cycle 10 (homologous to CD 2.12 CALU6_cells, DU145_cells, PC3_cells 109248 AA194720 Hs.189996 ESTs; Highly similar to sec61 homolog [H 2.12 HT29_cells, MB231_cells, HMEC (total RNA) 106724 AA465226 Hs.28631 ESTs 2.12 EB_cells, 293T_cells, DU145_cells 100571 HG2264-H Atpase, Ca2+ Transporting, Plasma Membra 2.12 EB_cells, Lu_AD_H23, Lu_SC_H69 133017 AA450187 Hs.178518 ESTs 2.12 OVCAR_cells, PC3_cells, 293T_cells 124313 H94650 Hs.108002 ESTs 2.12 MB-MDA-453, Lu_SC_H345, HT29_cells 113059 T26925 Hs.172684 vesicle-associated membrane protein 8 (e 2.12 MB-MDA-453, PC3_cells, LNCaP_cells 113241 T63313 Hs.226136 ESTs; Moderately similar to !!!! ALU SUB 2.12 HMEC (total RNA), BT474_cells, HMEC 111952 R40782 Hs.21296 ESTs 2.12 HT29_cells, PC3_cells, A549_cells 113965 W86519 Hs.19631 ESTs 2.12 PC3_cells, EB_cells, LNCaP_cells 108059 AA043944 Hs.62663 ESTs 2.12 EB_cells, OVCAR_cells, 293T_cells 124235 H63994 Hs.221134 ESTs 2.12 Fibroblasts 2, MB-MDA-453, PRSC_con 106400 AA447621 Hs.31257 ESTs 2.12 DU145_cells, EB_cells, Caco2 119590 W44798 Hs.55876 ESTs 2.12 PRSC_log, Lu_SC_H69, Lu_SC_H345 112434 R63068 Hs.159793 EST 2.11 HS578T_cells, LNCaP_cells, OVCAR_cells 122731 AA457549 aa92b1.s1 Stratagene fetal retina 93722 2.11 MB-MDA-453, RPWE_2, MCF7 gb:X5275_ma3 LEUKOSIALIN PRECURSOR (HU 115348 AA281562 Hs.88860 ESTs 2.11 EB_cells, Lu_AD_H23, Fibroblasts 2 128873 AA226768 Hs.109483 ESTs; Weakly similar to predicted using 2.11 MB-MDA-435s, EB_cells, LNCaP_cells 133742 T54301 Hs.75844 ESTs 2.11 EB_cells, CALU6_cells, DU145_cells 102099 U11870 Hs.194778 interleukln 8 receptor alpha 2.11 Lu_AD358, PC3_cells, PRSC_con 125840 H05787 Hs.12064 ubiquitin specific protease 22 2.11 EB_cells, LNCaP_celis, Caco2 106501 AA256604 Hs.31930 ESTs 2.1 Fibroblasts 2, HS578T_cells, MB-MDA-4355 111576 R10334 Hs.15489 ESTs 2.1 Lu_SC_H69, PRSC_log, Lu_SC_H345 104275 C02170 Hs.39387 ESTs; Weakly similar to weak similarity 2.1 HT29_cells, MB231_cells, Lu_SC_H69 117803 N48620 Hs.28483 pregnancy specific beta-1-glycoprotein 9 2.1 HT29_cells, HMEC, RPWE_2 122725 AA457407 Hs.152204 transmembrane protease; serine 2 2.1 Lu_SC_H69, Lu_LC_H450, Lu_SC_H345 120987 AA398233 Hs.111894 KIAA0108 gene product 2.1 Fibroblasts 2, PRSC_con, MCF7 105932 AA403305 Hs.12185 ESTs; Weakly similar to myosin phosphata 2.1 LNCaP_cells, MCF7, OVCAR_cells 118398 N64706 Hs.137282 ESTs 2.1 Lu_SC_H345, HT29_cells, HMEC 103679 Z86000 Human DNA seq from PAC 151B14 onchromos 2.1 CALU6_cells, A549_cells, Lu_SC_H345 receptor subtype 3 (SSTR3), tRNA, ESTs, 130303 L40392 Hs.180789 H sapiens (clone S164) mRNA; 3′ end of c 2.1 PC3_cells, DU145_cells, LNCaP_cells 122815 AA461080 Hs.139446 ESTs 2.1 HT29_cells, BT474_cells, MB231_cells 105598 AA279439 Hs.20594 ESTs; Weakly similar to misato [D.melano 2.1 EB₁₃ cells, Lu_SC_H345, LNCaP_cells 124889 R69088 Hs.28728 ESTs; Weakly similar to F55A12.9 [C.eleg 2.1 HT_cells, BT474_cells, MB231_cells 129599 F10720 Hs.180804 ESTs 2.1 HS578T_cells, HT29_cells, HT29_cells 110338 H40359 Hs.177256 ESTs 2.09 MCF7, A549_cells, MB-MDA-435s 134092 H17490 Hs.7905 ESTs: Highly similar to sorting nexin 9 2.09 EB_cells, Fibroblasts 2 HS578T_cells 133002 AF006082 Hs.62461 ARP2 (actin-related protein 2; yeast) ho 2.09 EB_cells, HS578T_cells, A549_cells 115570 AA398343 Hs.94943 ESTs 2.09 Lu_SC_H345, PC3_cells, LNCaP_cells 120055 W93299 Hs.59363 ESTs; Weakly similar to cytokeratin 20 [ 2.09 HMEC (total RNA), HS578T_cells, HS578T_cells 116332 AA491208 Hs.62620 ESTs 2.09 EB_cells, Lu_AD_H23, Lu_SC_H69 105415 AA243768 Hs.4232 ESTs; Highly similar to match to ESTs Z4 2.09 LNCaP_cells, Lu_AD_H23, MB-MDA-453 116607 D80354 Hs.256321 EST 2.09 LNCaP_cells, DU145_cells, RPWE_2 126731 AA593973 Hs.232217 ESTs; Weakly similar to !!!! ALU SUBFAMI 2.09 MB231_cells, HT29_cells, HMEC 102276 U30999 Hs.10247 activated leucocyte cell adhesion molecu 2.09 PC3_cells, HS578T_cells, DU145_cells 113666 T96077 Hs.17738 EST 2.09 Lu_AD_H23, Lu_AD_H23, Lu_SQ_H520 101183 L19779 Hs.795 H2A histone family; member O 2.09 LNCaP_cells, MCF7, OVCAR_cells 112177 R49025 Hs.22996 ESTs 2.09 Lu_AD_H23, Lu_AD_358, Lu_SC_H69 115038 AA252360 Hs.87968 ESTs 2.08 BT474_cells, MB231_cells, HT29_cells 109638 F04432 Hs.17904 ESTs 2.08 EB_cells, DU145_cells, PC3_cells 109592 F02475 Hs.26370 ESTs 2.08 Lu_AD_H23, Lu_SQ_H520, Lu_LC_H460 133740 U68142 Hs.170160 RAB2: member RAS oncogene family-like 2.08 LNCaP_cells, MB-MDA-453, EB_cells 126716 AA031700 Hs.251962 ESTs 2.08 HS578T_cells, Fibroblasts 2, Lu_SC_H69 124055 F10904 Hs.100516 H sapiens clone 23605 mRNA seq 2.08 Lu_SC_H345, OVCAR_cells, DU145_cells 113283 T66813 Hs.12947 EST 2.08 EB_cells, Lu_SC_H69, Lu_AD_H23 120097 W95068 Hs.59621 ESTs 2.08 HS578T_cells, A549_cells, CALU6_cells 102066 U08471 Hs.352 folate receptor 3 (gamma) 2.08 EB_cells, Lu_AD_H23, Lu_AD_358 108712 AA121993 zm24d11.s1 Stratagene pancreas (#93728) 2.08 Lu_SQ_H520, HT29_cells, BT474_cells similar to gb:Y433 GLUTATHIONE PEROXIDAS 134453 X70683 Hs.83484 SRY (sex determining region Y)-box 4 2.08 EB_cells, Lu_SC_H345, Lu_SC_H69 103883 AA232836 Hs.87363 ESTs 2.08 HT29_cells, 293T_cells, 293T_cells 105313 AA233856 Hs.16930 ESTs 2.08 DU145_cells, MB-MDA-435s, HS578T_cells 113669 T96148 Hs.17762 ESTs 2.08 EB_cells, Lu_SQ_H520, Fibroblasts 2 120380 AA227904 Hs.104223 ESTs 2.08 293T_cells, CALU6_cells, A549_cells 121045 AA398554 Hs.181012 double-stranded RNA-binding zinc finger 2.08 293T_cells, PC3_cells, OVCAR_cells 104949 AA070735 Hs.148090 ESTs 2.08 Lu_SC_H69, Lu_SC_H345, RPWE_2 118751 N74210 Hs.50454 EST 2.08 Lu_AD_H23, Lu_SC_H69, Lu_SC_H345 112399 R60920 Hs.26419 H sapiens clone 24510 mRNA seq 2.08 EB_cells, Lu_AD_H23, Lu_SC_H69 129994 AA599443 Hs.38194 ESTs; Moderately similar to !!!! ALU SUB 2.08 DU145_cells, EB_cells, HS578T_cells 116402 AA600054 Hs.65302 ESTs 2.08 HT29_cells, BT474_cells, Lu_AD_H23 125307 Z40583 Hs.101259 ESTs 2.08 HMEC, HMEC (total RNA), EB_cells 105047 AA132453 Hs.15396 ESTs 2.08 Caco2, HT29_cells, LNCaP_cells 128659 T95280 Hs.103315 trinucleotide repeat containing 1 2.08 EB_cells, Lu_AD_H23, Lu_SC_H69 122301 AA437378 Hs.98791 ESTs 2.08 Lu_SC_H345, Lu_AD_H23, Lu_AD_358 121974 AA429804 Hs.229675 EST 2.08 HS578T_cells, 293T_cells, OVCAR_cells 116905 H71420 ys8c12.s1 Soares fetal liver spleen 1NFL 2.08 Lu_AD_H23, EB_cells, PRSC_con 3′ similar to contains Alu repetitive e 106703 AA463979 Hs.21264 KIAA0782 protein 2.08 EB_cells, Caco2, PRSC_con 121908 AA427858 Hs.98534 EST 2.07 293T_cells, Lu_SC_H345, CALU6_cells 135119 T23992 Hs.94769 ESTs; Moderately similar to RAS-RELATED 2.07 HS578T_cells, PRSC_con, OVCAR_cells 103558 Z19574 Hs.2785 keratin 17 2.07 RPWE_2, HMEC (total RNA), HMEC 124209 H57317 Hs.193433 ESTs 2.07 Fibroblasts 2, OVCAR_cells, 293T_cells 133936 AA045083 Hs.77719 gamma-glutamyl carboxylase 2.07 Fibroblasts 2, MB-MDA-453, PRSC_con 116246 AA479961 Hs.42913 ESTs; Highly similar to ubiquilin-conjug 2.07 EB_cells, LNCaP_cells, LNCaP_cells 123230 AA490134 Hs.105308 EST 2.07 Lu_AD_H23, Lu_SC_H69, Lu_SC_H345 127378 AA452696 zx39b05.r1 Soares_total_fetus_Nb2HF8_9w 2.07 HS578T_cells, LNCaP_cells, EB_cells to contains Alu repetitive element; cont 110464 H53013 Hs.221901 ESTs 2.07 Fibroblasts 2, Lu_SQ_H520, Lu_SQ_H520 135191 X07619 Hs.169876 cytochrome P450; subfamily IID (debrisoq 2.07 Lu_AD_H23, Lu_SC_H69, Lu_AD_358 polypeptide 7a (pseudogene) 101267 L36818 Hs.75339 inositol polyphosphate phosphatase-like 2.07 Lu_SC_H345, OVCAR_cells, Caco2 105185 AA191495 Hs.189937 ESTs 2.07 Lu_SC_H69, Lu_AD_H23, Lu_SC_H345 125366 H60192 Hs.76853 ESTs; Weakly similar to human homolog of 2.07 DU145_cells, Lu_LC_H460, Lu_AD_358 117472 N30131 Hs.93738 DKFZP434M098 protein 2.07 EB_cells, Lu_SC_H69, 293T_cells 114235 Z39710 Hs.25341 ESTs 2.07 DU145_cells, BT474_cells, Lu_SC_H69 109081 AA165268 Hs.72488 ESTs 2.07 Lu_SC_H69, Lu_SC_H345, PC3_cells 112596 R78212 Hs.163705 ESTs 2.07 MB-MDA-435s, Lu_SQ_H520, MB-MDA-453 109254 AA194940 Hs.85956 ESTs; Weakly similar to line-1 protein O 2.07 HS578T_cells, 293T_cells, OVCAR_cells 105898 AA401144 Hs.27354 ESTs 2.07 EB_cells, 293T_cells, PRSC_con 116290 AA488691 Hs.57969 phenylalanine-tRNA synthetase 2.06 Lu_AD_H23, Lu_SC_H345, PRSC_log 122529 AA449828 Hs.99229 ESTs 2.06 DU145_cells, HS578T_cells, 293T_cells 104612 R99199 Hs.173063 transducin-like enhancer of split 2: hom 2.06 MB-MDA-435s, 293T_cells, 293T_cells 116465 AA621650 Hs.41045 ESTs; Weakly similar to KIAA0734 protein 2.06 MB231_cells, HT29_cells, Lu_AD_358 123155 AA488414 Hs.76127 hect (homologous to the E6-AP (UBE3A) ca 2.06 DU145_cells, CALU6_cells, PC3_cells domain (RLD) 1 126752 AI073373 Hs.183275 ESTs 2.06 LNCaP_cells, EB_cells, DU145_cells 126455 N80749 Hs.111515 ESTs; Weakly similar to predicted using 2.06 CALU6_cells, PRSC_log, OVCAR_cells 129339 R77869 Hs.28506 ESTs 2.06 EB_cells, BT474_cells, Lu_AD_H23 115021 AA252028 Hs.39168 ESTs 2.06 Lu_SQ_H520, Fibroblasts 2, EB_cells 129054 T67231 Hs.168289 succinate dehydrogenase complex; subunit 2.06 Caco2, LNCaP_cells, EB_cells 101261 L35545 Hs.82353 endothelial cell protein C/activated pro 2.06 EB_cells, RPWE_2, DU145_cells 132697 AA281951 Hs.5518 H sapiens mRNA; cDNA DKFZp566J2146 (from 2.06 OVCAR_cells, LNCaP_cells, DU145_cells 124380 N26536 Hs.84999 ATPase; Cu++ transporting; beta polypept 2.06 Caco2, Caco2, 293T_cells 103967 AA303711 Hs.144700 ephrin-B1 2.06 HT29_cells, HMEC (total RNA), HMEC 119403 T92935 Hs.119908 ESTs; Highly similarto nucleolar protei 2.06 HMEC, EB_cells, HMEC (total RNA) 125755 R66080 Hs.191268 H sapiens mRNA; cDNA DKFZp434N174 (from 2.06 LNCaP_cells, DU145_cells, OVCAR_cells 101843 M93405 Hs.170008 methylmalonate-semialdehyde dehydrogenas 2.05 LNCaP_cells, MB-MDA-453, EB_cells 113032 T24024 Hs.7387 DKFZPS64B116 protein 2.05 EB_cells, A549_cells, A549_cells 112563 R72632 Hs.29282 ESTs 2.05 MCF7, HS578T_cells, PRSC_con 126432 AA583825 Hs.235860 ESTs 2.05 MB231_cells, HT29_cells, Fibroblasts 2 101636 M57763 Hs.89474 ADP-ribosylation factor 6 2.05 DU145_cells, LNCaP_cells, PC3_cells 125174 W51835 Hs.231082 EST 2.05 26_cells, Fibroblasts 2, Lu_AD_H23 106168 AA425943 Hs.82208 acyl-Coenzyme A dehydrogenase; very long 2.05 OVCAR_cells, PC3_cells, EB_cells 135343 AA236796 Hs.9914 follistatin 2.05 HMEC (total RNA), PC3_cells, HMEC 105267 AA227956 Hs.25348 follistatin-like 3 (secreted glycoprotel 2.05 HMEC, RPWE_2, HMEC (total RNA) 134331 AA452020 Hs.234156 ESTs; Weakly similar to CGI-128 protein 2.05 EB_cells, CALU6_cells, A549_cells 121634 AA417012 Hs.28921 ESTs 2.05 HS578T_cells, EB_cells, Lu_SC_H345 131394 R72637 Hs.26343 ESTs 2.05 EB_cells, Lu_SC_H69, Lu_AD_H23 111526 R05260 Hs.20131 ESTs 2.05 Lu_AD_H23, Lu_SC_H69, BT474_cells 125049 T79840 Hs.111798 ESTs 2.05 HT29_cells, Lu_AD_H23, Lu_SC_H345 120433 AA237077 Hs.180777 H sapiens mRNA; cDNA DKFZp564M0264 (from 2.05 DU145_cells, CALU6_cells, PC3_cells 129498 AA449789 Hs.75511 connective tissue growth factor 2.05 HS578T_cells, PRSC_log, PRSC_con 127805 AA740921 Hs.1197 heat shock 10 kD protein 1 (chaperonin 10 2.05 DU145_cells, LNCaP_cells, OVCAR_cells 109275 AA196287 Hs.20303 ESTs; Moderately similar to !!!! ALU SUB 2.05 EB_cells, MB-MDA-453, Fibroblasts 2 120683 AA290987 Hs.49657 ESTs; Weakly similar to contains similar 2.04 Lu_AD_358, Lu_SQ_H520, Lu_LC_H460 135415 X60655 Hs.99967 even-skipped homeo box 1 (homolog of Dro 2.04 Lu_AD_H23, RPWE_2, Lu_SQ_H520 132925 AA252759 Hs.238296 DKFZP434A033 protein 2.04 293T_cells, HS578T_cells, LNCaP_cells 101875 M97287 Hs.74592 special AT-rich seq binding protein 1 (b 2.04 EB_cells, Lu_SC_H69, 293T_cells 101453 M22490 Hs.65879 bone morphogenetic protein 4 2.04 PRSC_con, HT29_cells, MB231_cells 129177 T95005 Hs.209587 ESTs 2.04 293T_cells, MB-MDA-435s, Lu_SC_H69 130726 W55946 Hs.18508 putative glycine-N-acyltransferase 2.04 HT29_cells, Fibroblasts 2, MB-MDA-435s 105549 AA262417 Hs.5415 ESTs 2.04 DU145_cells, OVCAR_cells, PC3_cells 124543 N63706 Hs.104573 ESTs 2.04 Caco2, 293T_cells, DU145_cells 123062 AA482069 Hs.100847 ESTs 2.04 Lu_AD_358, HT29_cells, HT29_cells 109464 AA232557 Hs.87100 ESTs 2.04 DU145_cells, Lu_AD_H23, LNCaP_cells 129619 AA610116 Hs.11663 tetraspan NET-6 protein 2.04 BT474_cells, Caco2, LNCaP_cells 127545 AA935809 Hs.115899 ESTs 2.04 BT474_cells, MB-MDA-4355, MB-MDA-453 133068 R73427 Hs.235712 ESTs 2.04 Caco2, OVCAR_cells, MCF7 113609 T93263 Hs.16875 ESTs; Weakly similar to hypothetical pro 2.04 EB_cells, Lu_SC_H345, PRSC_con 106645 AA460270 Hs.27695 midline 1 (Opitz/BBB syndrome) 2.04 A549_cells, 293T_cells, Caco2 126256 Z21124 HSAAADNVE TEST1, Human adult Testis tiss 2.04 Fibroblasts 2, Fibroblasts 2, MCF7 129697 R00541 Hs.172069 DKFZP434C212 protein 2.04 HT29_cells, Lu_SQ_H520, BT474_cells 126730 T19477 A1426R Heart H sapiens cDNA clone A1426, 2.04 EB_cells, Lu_AD_H23, Lu_SC_H69 125244 W86466 Hs.132756 ESTs; Weakly similar to KIAA0591 protein 2.04 EB_cells, Lu_AD_H23, Lu_LC_H460 134762 M91036 Hs.242985 hemoglobin; gamma G 2.04 MB231_cells, Lu_AD_358, HT29_cells 119564 W38206 Accession not listed in Genbank 2.04 BT474_cells, HT29_cells, Lu_AD_H23 132523 AB002332 Hs.50722 clock (mouse) homolog 2.04 PC3_cells, OVCAR_cells, PRSC_log 127758 AI337031 Hs.180195 ESTs 2.04 293T_cells, MB-MDA-435s, A549_cells 126471 AA158755 Hs.175652 ESTs; Weakly similar to !!!! ALU SUBFAMI 2.04 EB_cells, Lu_AR_358, Lu_LC_H460 110911 N45120 Hs.22305 ESTs 2.03 Lu_AD_H23, RPWE_2, Lu_LC_H460 122317 AA442742 Hs.8693 ESTs; Weakly similar to !!!! ALU SUSFAMI 2.03 EB_cells, Fibroblasts 2, Lu_SC_H345 100253 D38024 Hs.247951 Humn facioscapulohumeral muscular dystro 2.03 Lu_AD_H23, Lu_AD_358, Lu_SQ_H520 120431 AA236854 Hs.247323 H sapiens mRNA for G4 protein (G4 gene; 2.03 Lu_SQ_H69, EB_cells, Lu_SC_H345 122449 AA447638 Hs.104977 ESTs 2.03 Lu_SC_H345, Lu_SC_H345, Lu_SQ_H520 100961 J00148 Accession not listed in Genbank 2.03 HT29_cells, BT474_cells, HMEC 130908 W86389 Hs.21122 ESTs; Moderately similar to KIAA0438 [H. 2.03 293T_cells, Lu_SC_H345, OVCAR_cells 102643 U67649 Human bota-galactoside alpha2,6-sialyltr 2.03 HT29_cells, 293T_cells, Lu_SC_H345 127932 AA398510 Hs.133148 ESTs 2.03 EB_cells, Lu_SC_H345, Lu_SC_H69 109207 AA190906 Hs.204692 ESTs 2.03 Lu_SQ_H520, Lu_SQ_H345, Lu_SC_H69 102598 U62962 Hs.106673 eukatyotic translation initiation factor 2.03 EB_cells, DU145_cells, MCF7 124470 N51702 Hs.101392 ESTs 2.03 HT29_cells, Fibroblasts 2, HMEC (total RNA) 104961 AA076672 Hs.33905 ESTs 2.03 Caco2, LNCaP_cells, EB_cells 124164 H30667 Hs.7535 ESTs; Highly similar to COBW-like placen 2.03 CALU6_cells, CALU6_cells, A549_cells 126468 AA242853 Hs.237856 ESTs; Moderately similar to cAMP inducib 2.03 MB231_cells, BT474_cells, Fibroblasts 2 129683 W05348 Hs.158196 DKFZP434B103 protein 2.03 HT29_cells, MB-MDA-435s, Lu_AD_H23 105350 AA235737 Hs.186571 ATPase; Na+/K+ transporting; alpha 3 pol 2.03 MB-MDA-453, Lu_SQ_H520, Lu_AD_358 129794 AA447772 Hs.14520 eukaryotic translation initiation factor 2.03 EB_cells, Lu_AD_358, Lu_AD_H23 115664 AA405974 Hs.54673 tumor necrosis factor (ligand) superfami 2.03 Lu_AD_358, HT29_cells, HT29_cells 119096 R41672 Hs.91471 ATPase type IV; phospholipid transportin 2.03 HT29_cells, MB231_cells, BT474_cells 133866 L36151 Hs.171625 phosphatidylinositol 4-kinase; catalytic 2.03 293T_cells, DU145_cells, LNCaP_cells 132055 N69440 Hs.38132 ESTs 2.03 Lu_SC_H345, MB-MDA-453, MB-MDA-435s 125691 AI034361 Hs.135150 lung type-I cell membrane-associated gly 2.03 Lu_SC_H345, LNCaP_cells, DU145_cells 121376 AA405699 Hs.166232 ESTs; Moderately similar to SODIUM-AND 2.03 LNCaP_cells, HT29_cells, RPWE_2 TRANSPORTER 2 [H.sapiens] 105289 AA233178 Hs.103000 KIAA0831 protein 2.02 PC3_cells, Lu_AD_H23, MB231_cells 100967 J02621 Hs.251064 high-mobility group (nonhistone chromoso 2.02 MCF7, DU145_cells, OVCAR_cells 124430 N38913 Hs.221575 ESTs 2.02 MB-MDA-435s, Fibroblasts 2, EB_cells 128322 AI306331 Hs.133296 ESTs 2.02 HT29_cells, MB-MDA-435s, Lu_SC_H345 131077 X91809 Hs.22698 G alpha interacting protein 2.02 Lu_AD_H23, RPWE_2, MCF7 108033 AA040923 Hs.92200 KIAA0480 gene product 2.02 MCF7, Fibroblasts 2, DU145_cells 107550 AA001045 Hs.46783 ESTs 2.02 DU145_cells, PC3_cells, OVCAR_cells 109475 AA233159 Hs.87131 ESTs 2.02 HT29_cells, MB-MDA-435s, Lu_SC_H69 111400 R00144 Hs.189771 ESTs 2.02 HT29_cells, Fibroblasts 2, HMEC 117516 N32495 Hs.151560 ESTs 2.02 HT29_cells, HMEC (total RNA), Fibroblasts 2 120506 AA257955 Hs.173705 ESTs; Weakly similar to !!!! ALU CLASS C 2.02 MCF7, Fibroblasts 2, LNCaP_cells 130850 N39308 Hs.20237 DKFZPS66C134 protein 2.02 EB_cells, Lu_AD_H23, Lu_LC_H460 123118 AA486571 Hs.105696 ESTs; Moderately similarto !!!! ALU SUB 2.02 CALU6_cells, 293T_cells, PRSC_log 111285 N71704 Hs.4310 eukaryotic translation initiation factor 2.02 293T_cells, PC3_cells, EB_cells 119106 R42362 Hs.91785 ESTs 2.02 CALU6_cells, MB-MDA-453, PC3_cells 111370 N92915 Hs.94031 brefeldin A-inhibited guanine nucleotide 2.02 EB_cells, OVCAR_cells, LNCaP_cells 125013 T67261 Hs.154431 ESTs; Weakly similarto neuronal thread 2.02 Lu_SC_H345, Lu_SC_H69, PRSC_con 129762 AA460273 Hs.12372 KIAA0517 protein 2.02 EB_cells, MB-MDA-435s, OVCAR_cells 120704 AA291970 Hs.107054 KIAA0821 protein 2.01 Lu_SC_H69, EB_cells, MB-MDA-453 105355 AA235985 Hs.26938 Human DNA seq from clone 126A5 on chromo 2.01 Lu_AD_H23, Lu_LC_H460, Lu_SQ_H520 genes (one with DnaJ domains); the gene family member HKR3. Contains ESTs; STSs; 125952 AA017723 small inducible cytokine A5 (RANTES) 2.01 LNCaP_cells, DU145_cells, MB231_cells 103478 Y07755 Hs.38991 S100 calcium-binding protein A2 2.01 HMEC (total RNA), HMEC, RPWE_2 133544 T33873 Hs.74624 protein tyrosine phosphatase; receptor t 2.01 Lu_SC_H345, BT474_cells, HT29_cells 112746 R93237 yq11e10.s1 Soares fetal liver spleen 1NF 2.01 PC3_cells, LNCaP_cells, OVCAR_cells IMAGE: 196650 3′, mRNA seq. 118513 N67504 Hs.40061 ESTs 2.01 Lu_SC_H345, Lu_SC_H69, PRSC_con 123423 AA598484 Hs.238476 EST 2.01 EB_cells, Lu_AD_H23, Lu_SC_H345 127854 AA769520 ESTs; Weakly similar to REGULATOR OF MIT 2.01 HS578T_cells, CALU6_cells, Lu_SQ_H520 111843 R36969 Hs.18888 ESTs 2.01 Lu_AD_H23, Lu_AD_358, Lu_SQ_H520 100221 D28383 Human mRNA for ATP synthase B chain, 5′U 2.01 EB_cells, Lu_AD_H23, LNCaP_cells 129968 AA452237 Hs.194443 ESTs; Weakly similar to BC37295_2 [H.sap 2.01 Lu_SC_H345, Lu_SC_H69, DU145_calls 106798 AA478968 Hs.20558 ESTs 2.01 EB_cells, Lu_AD_H23, Lu_LC_H460 114636 AA085374 zn13dS.s1 Stratagene hNT neuron (#937233 2.01 EB_cells, CALU6,_cells, OVCAR_cells gb:L8441 CYTOCHROME C OXIDASE POLYPEPTI 125348 H21585 Hs.191277 ESTs; Moderately similar to ATP binding 2.01 EB_cells, HS578T_cells, PC3_cells 130620 AA233245 Hs.16773 ESTs 2.01 EB_cells, DU145_cells, 293T_cells 106471 AA450118 Hs.25722 ESTs; Weakly similar to ZINC FINGER PROT 2.01 OVCAR_cells, LNCaP_cells, EB_cells 134175 T33128 Hs.7966 ESTs 2 Lu_SC_H345, Fibroblasts 2, Lu_AD_H23 117291 N22289 yw36g08.s1 Morton Fetal Cochlea H sapien 2 MB-MDA-453, OVCAR_cells, CALU6_cells 134199 U47635 Hs.79877 myotubularin related protein 6 2 EB_cells, PC3_cells, LNCaP_cells 128758 AA129545 Hs.181165 eukaryotic translation elongation factor 2 Lu_SC_H69, EB_cells, Lu_SC_H345 112005 R42569 Hs.22444 ESTs 2 Lu_AD_H23, PRSC_log, Lu_AD_358 122521 AA449433 Hs.149227 ESTs; Weakly similar to PROLINE-RICH PRO 2 HT29_cells, RPWE_2, MB231_cells 130368 X84373 Hs.155017 nuclear receptor interacting protein 1 2 DU145_cells, PC3_cells, MCF7 114067 Z38153 Hs.26921 ESTs 2 293T_cells, MB-MDA-435s, HT29_cells 107136 AA620795 Hs.8207 ESTs 2 LNCaP_cells, PC3_cells, EB_cells

[0329] TABLE 3 Pkey: Unique Eas probeset identifier number ExAcon: Exemplar Accession number, Genbank accession number UnigeneID: Unigene number Unigene Title: Unigene gene title Ratio Pkey Ex Accn UG_ID Complete_Title BS/Met Top 3 expressing cell lines 302347 AF039400 Hs.194059 chloride channel; calcium activated; fam 19.71 EB, NCI-H520, NCI-H23 316304 AI936587 Hs.221599 ESTs 14.49 PRSC_con, RPWE-2, OVCA-R 339196 CH22_FF113D11.GENSCAN.3-1 10.37 NCI-H69, PRSC_con, NCI-H345 336171 CH22_FGENES.708_3 9.45 NCI-H69, NCI-H460, NCI-H23 338895 CH22_DJ32I10.GENSCAN.9-2 9.31 PC3, BT474, OVCA-R 333625 CH22_FGENES.223_2 8.96 NCI-H69, PRSC_con, NCI-H345 333730 CH22_FGENES.258_1 8.82 NCI-H69, BT474, MB-MDA-231 320244 AA296922 Hs.129778 gastrointestinal peptide 8.22 BT474, CALU6, DU145 333643 CH22_FGENES.232_2 7.66 MCF7, NCI-H69, LnCap 333423 CH22_FGENES.147_3 7.57 HT29, MB-MDA-231, EB 302332 AI833168 Hs.184507 H sapiens Chromosome 16 BAC clone CIT987 7.55 MB-MDA-231, HT29, MB-MDA-453 333588 CH22_FGENES.206_2 7.46 HT29, OVCA-R, BT474 322033 AL137507 EST cluster (not in UniGene) 7.35 PRSC_con, PRSC_log, NCI-H345 308601 AI719930 EST singleton (not in UniGene) with exon 6.83 PC3, DU145, DU145 339044 CH22_DA59H18.GENSCAN.27-5 6.46 NCI-H69, NCI-H345, PRSC_log 314516 AA371513 Hs.231748 ESTs 6.41 EB, OVCA-R, Caco2 327805 CH.05_hs gi|5867968 6.28 NCI-H69, NCI-H345, PRSC_con 334239 CH22_FGENES.364_2 6.09 NCI-H520, MB-MDA-435s, MB-MDA-453 332958 CH22_FGENES.48_15 6.04 NCI-H69, PRSC_con, PRSC_log 313386 W85772 Hs.173924 ESTs 5.88 MB-MDA-231, OVCA-R, BT474 314350 AL037927 Hs.190675 ESTs; Moderately similar to !!!! ALU SUB 5.84 OVCA-R, CALU6, EB 337170 CH22_FGENES.564-1 5.67 LnCap, CALU6, NCI-H69 337503 CH22_FGENES.803-1 5.66 NCI-H345, PRSC_con, RPWE-2 337562 CH22_C65E1.GENSCAN.1-2 5.53 HT29, MB-MDA-453, BT474 337219 CH22_FGENES.614-3 5.45 NCI-H69, NCI-H345, PRSC_log 311331 AI679622 Hs.32225 immunoglobulin alpha 1 5.43 NCI-H69, NCI-H23, NCI-H345 314251 AA713589 EST cluster (not in UniGene) 5.41 PC3, EB, LnCap 336246 CH22_FGENES.746_5 5.34 NCI-H69, NCI-H345, PRSC_log 335009 CH22_FGENES.472_13 5.31 ES, EB, NCI-H69 339365 CH22_BA354I12.GENSCAN.34-1 5.25 PRSC_con, NCI-H69, PRSC_log 336088 CH22_FGENES.688_17 5.21 PRSC_con, Caco2, PRSC_log 334966 CH22_FGENES.465_36 5.16 DU145, BT474, MB-MDA-231 334666 CH22_FGENES.418_18 5.15 NCI-H69, NCI-H345, PRSC_log 316830 AW182106 Hs.127821 ESTs 5.12 NCI-H345, PRSC_con, PRSC_log 339413 CH22_DJ579N16.GENSCAN.5-8 5.06 NCI-H69, NCI-H345, PRSC_log 337951 CH22_EM:AC005500.GENSCAN.94-1 5.01 NCI-H345, NCI-H69, PRSC_con 330153 CH21_p2 gi|4325335 5 PRSC_con, PRSC_log, NCI-H69 333987 CH22_FGENES.310_11 4.96 MB-MDA-231, MB-MDA-453, MB-MDA-453 334304 CH22_FGENES.373_7 4.96 OVCA-R, CALU6, NCI-H23 338990 CH22.DA59H18.GENSCAN.6-6 4.95 PRSC_log, PRSC_con, NCI-H69 333152 CH22_FGENES.89_1 4.89 MB-MDA-435s, OVCA-R, A549 327049 CH.21_hs gi|6531965 4.87 PRSC_con, NCI-H345, PRSC_log 337225 CH22_FGENES.626-3 4.83 DU145, CALU6, EB 333496 CH22_FGENES.168_6 4.81 NCI-H69, NCI-H345, PRSC_con 334451 CH22_FGENES.387_11 4.79 RPWE-2, PRSC_con, NCI-H69 333594 CH22_FGENES.210_3 4.78 OVCA-R, PC3, HT29 333635 CH22_FGENES.228_2 4.78 NCI-H69, PRSC_log, PRSC_con 336796 CH22.FGENES.176-6 4.73 NCI-H69, NCI-H345, PRSC_log 333313 CH22_FGENES.138_5 4.72 NCI-H69, NCI-H345, PRSC_log 336833 CH22_FGENES.242-2 4.7 NCI-H345, NCI-H69, PRSC_con 336090 CH22_FGENES.689_2 4.7 NCI-H69, PRSC_con, PRSC_log 336645 CH22_FGENES.26-1 4.63 HT29, OVCA-R, DU145 334565 CH22_FGENES.405_5 4.62 NCI-H345, PRSC_log, RPWE-2 333242 CH22_FGENES.111_6 4.56 NCI-H345, PRSC_log, PRSC_con 326304 CH.17_hs gi|5867277 4.48 OVCA-R, EB, DU145 337445 CH22_FGENES.769-4 4.47 RPWE-2, NCI-H69, PRSC_log 327413 CH.02_hs gi|5867750 4.46 NCI-H69, PRSC_log, NCI-H345 327990 CH.06_hs gi|5868218 4.44 PRSC_con, PRSC_log, RPWE-2 325038 H38304 Hs.21782 ESTs 4.43 PRSC_con, MB-MDA-231, HT29 314923 AI732489 Hs.136370 ESTs 4.4 HT29, MB-MDA-231, NCI-358 328859 CH.07_hs gi|6381928 4.4 OVCA-R, BT474, A549 334476 CH22_FGENES.394_7 4.38 OVCA-R, PC3, EB 336092 CH22_FGENES.689_6 4.35 PRSC_con, Caco2, PRSC_log 333965 CH22_FGENES.305_3 4.35 NCI-H69, NCI-H345, PRSC_log 336402 CH22.FGENES.823_17 4.34 RPWE-2, HT29, OVCA-R 337947 CH22_EM:AC005500.GENSCAN.90-5 4.33 OVCA-R, DU145, PC3 337504 CH22_FGENES.803-2 4.33 NCI-H345, PRSC_con, PRSC_log 336813 CH22_FGENES.213-6 4.33 DU145, HT29, OVCA-R 338069 CH22_EM:AC005500.GENSCAN.166-14 4.33 NCI-H69, PRSC_con, NCI-H345 318538 N28625 Hs.74034 caveolin 1; caveolae protein; 22 kD 4.31 PC3, A549, BT474 333631 CH22_FGENES.227_2 4.3 OVCA-R, PRSC_con, LnCap 302646 M14268 EST 4.27 PRSC_con, PRSC_log, RPWE-2 336049 CH22.FGENES.681_2 4.26 HT29, DU145, DU145 335667 CH22_FGENES.590_18 4.25 NCI-H520, Caco2, MB-MDA-453 320352 Y13323 Hs.145296 disintegrin protease 4.25 MB-MDA-231, DU145, BT474 304480 AA430373 EST singleton (not in UniGene) with exon 4.22 NCI-358, NCI-H460, NCI-H23 327273 CH.01_hs gi|5867466 4.22 NCI-H69, NCI-H345, PRSC_con 334540 CH22FGENES.403_5 4.17 NCI-H69, NCI-H345, PRSC_log 334719 CH22_FGENES.421_30 4.17 NCI-H69, NCI-H345, RPWE-2 327827 CH.05_hs gi|5867968 4.17 OVCA-R, NCI-H69, CALU6 333599 CH22_FGENES.212_2 4.17 PRSC_log, NCI-H69, PRSC_con 329638 CH.12_p2 gi|3779004 4.16 DU145, MB-MDA-231, HT29 307556 AI281651 EST singleton (not in UniGene) with exon 4.16 BT474, HT29, CALU6 336836 CH22_FGENES.247-11 4.15 PRSC_con, NCI-H345, NCI-H69 323187 AL121180 Hs.240038 ESTs 4.14 NCI-H345, MB-MDA-435s, RPWE-2 336397 CH22_FGENES.823.12 4.13 NCI-H345, PRSC_con, RPWE-2 325007 AA736429 EST cluster (not in UniGene) 4.13 NCI-H69, PRSC_con, NCI-H345 300199 AI304386 Hs.150836 ESTs 4.11 NCI-H345, PRSC_con, PRSC_log 335832 CH22_FGENES.620_6 4.08 NCI-H69, NCI-H345, PRSC_log 312778 AI631655 Hs.197919 ESTs 4.07 NCI-358, NCI-H23, PRSC_con 323154 AA765301 Hs.151858 ESTs 4.06 NCI-H23, A549, HT29 315871 AW135312 Hs.117237 ESTs 4.05 MB-MDA-231, EB, MCF7 337452 CH22_FGENES.775-1 4.02 PRSC_con, PRSC_log, NCI-H345 335265 CH22_FGENES.521_1 4.01 NCI-H69, MCF7, RPWE-2 335200 CH22_FGENES.508_9 4.01 NCI-H69, PRSC_log, PRSC_con 336917 CH22_FGENES.346-4 3.99 PRSC_con, NCI-H345, PRSC_log 336584 CH22_FGENES.847_1 3.98 PRSC_log, PRSC_con, RPWE-2 333382 CH22_FGENES.143_21 3.97 EB, A549, HT29 329436 CH.Y_hs gi|5868883 3.97 BT474, PC3, HT29 336929 CH22_FGENES.349-3 3.94 NCI-H69, NCI-H345, PRSC_log 337238 CH22.FGENES.641-3 3.92 NCI-H69, NCI-H345, PRSC_log 333875 CH22.FGENES.291_11 3.92 PRSC_con, RPWE-2, PRSC_log 337069 CH22_FGENES.448.2 3.9 NCI-H69, LnCap, RPWE-2 332491 M24470 Hs.1435 guanosine monophosphate reductase 3.86 OVCA-R, MB-MDA-435s, CALU6 304623 AA521331 EST singleton (not in UniGene) with exon 3.86 OVCA-R, DU145, PC3 335348 CH22_FGENES.537_4 3.85 HT29, MB-MDA-231, PC3 334568 CH22_FGENES.405_9 3.85 NCI-H69, NCI-H345, PRSC_log 336924 CH22.FGENES.347-9 3.84 NCI-H345, PRSC_log, RPWE-2 301654 H81795 EST 3.84 NCI-H520, LnCap, NCI-358 334677 CH22_FGENES.418_30 3.83 PRSC_con, NCI-H345, NCI-H69 326688 CH.20.hs gi|5867582 3.83 NCI-H345, PRSC_con, PRSC_log 327790 CH.05_hs gi|5867977 3.8 PRSC_con, PRSC_log, NCI-H345 334591 CH22_FGENES.408_1 3.8 NCI-H69, PRSC_log, NCI-H345 337974 CH22_EM:AC005500.GENSCAN.106-3 3.78 PRSC_log, PRSC_con, NCI-H345 311274 AW293128 Hs.197101 ESTs 3.78 NCI-H345, PRSC_con, RPWE-2 326668 CH.20_hs gi|6552455 3.78 NCI-H345, NCI-H69, PRSC_log 304195 N35382 EST singleton (not in UniGene) with exon 3.77 NCI-H69, RPWE-2, PRSC_con 336294 CH22_FGENES.786_4 3.77 PRSC_con, PRSC_log, NCI-H69 311613 AL046311 Hs.252443 ESTs; Weakly similar to !!!! ALU SUBFAMI 3.76 HT29, BT474, MB-MDA-231 338123 CH22_EM:AC005500.GENSCAN.195-5 3.75 MB-MDA-231, HT29, BT474 318230 AA558125 EST cluster (not in UniGene) 3.74 RPWE-2, PRSC_con, NCI-H345 303985 AW514501 Hs.156110 Immunoglobulin kappa variable 1D-8 3.73 MB-MDA-231, BT474, PRSC_con 336502 CH22_FGENES.833_8 3.72 NCI-H345, RPWE-2, PRSC_con 334063 CH22_FGENES.327_17 3.71 NCI-H69, NCI-H345, PRSC_con 333600 CH22_FGENES.213_2 3.7 NCI-H69, OVCA-R, PC3 339424 CH22_DJ579N16.GENSCAN.14-3 3.69 NCI-H69, NCI-H345, PRSC_con 336862 CH22_FGENES.297-2 3.67 NCI-H345, PRSC_con, PRSC_log 334823 CH22.FGENES.437_5 3.67 RPWE-2, PRSC_log, PRSC_con 329940 CH.16_p2 gi|6165199 3.66 CALU6, EB, MCF7 300275 A1632123 Hs.231521 ESTs 3.66 PRSC_con, NCI-H69, RPWE-2 328820 CH.07_hs gi|5868330 3.66 NCI-H69, NCI-H345, PRSC_con 332398 AA446446 Hs.104788 H sapiens clone 24554 unknown mRNA 3.66 PRSC_con, PRSC_log, NCI-H345 325791 CH.14_hs gi|6682476 3.65 NCI-H345, BT474, LnCap 300672 R14469 Hs.258573 ESTs 3.65 MCF7, MB-MDA-453, MB-MDA-435s 338344 CH22_EM:AC005500.GENSCAN.312-8 3.65 NCI-H345, PRSC_log, PRSC_con 333257 CH22_FGENES.118_5 3.65 DU145, EB, OVCA-R 332140 AA620724 Hs.112890 ESTs 3.65 MB-MDA-453, DU145, MCF7 337489 CH22_FGENES.799-2 3.63 NCI-H345, NCI-H69, PRSC_log 305167 AA663080 EST singleton (not in UniGene) with exon 3.63 OVCA-R, MB-MDA-231, MB-MDA-435s 336200 CH22_FGENES.719_4 3.61 NCI-H69, PRSC_log, NCI-H345 339208 CH22_FF113D11.GENSCAN,6-3 3.59 PRSC_con, NCI-H69, PRSC_log 320090 AB002058 Hs.113275 purinergic receptor P2X-Iike 1; orphan r 3.58 OVCA-R, LnCap, NCI-H69 335999 CH22_FGENES.657_1 3.57 NCI-H345, NCI-H69, PRSC_con 332909 CH22_FGENES.36_13 3.57 NCI-H345, PRSC_con, PRSC_log 306531 AA991423 EST singleton (not in UniGene) with exon 3.56 BT474, MB-MDA-453, MB-MDA-435s 333261 CH22_FGENES.119_1 3.55 HT29, CALU6, MB-MDA-231 303883 AA176396 Hs.169624 ESTs 3.54 NCI-H69, NCI-H345, RPWE-2 335831 CH22_FGENES.620_5 3.53 MCF7, BT474, OVCA-R 333983 CH22_FGENES.310_7 3.52 NCI-H345, PRSC_con, PRSC_log 333623 CH22_FGENES.222_2 3.51 NCI-H69, PRSC_con, PRSC_log 333997 CH22_FGENES.310_22 3.5 NCI-H345, PRSC_con, PRSC_log 325623 CH.14_hs gi|5867000 3.5 CALU6, HT29, BT474 309151 AI935829 Hs.140 immunoglobulin gamma 3 (Gm marker) 3.49 EB, MCF7, MB-MDA-453 305080 AA641485 EST singleton (not in UniGene) with exon 3.49 NCI-H23, NCI-H460, NCI-358 339268 CH22_BA354I12.GENSCAN.10-6 3.47 NCI-H69, NCI-H345, PRSC_con 310048 AI198352 Hs.105077 ESTs 3.47 Caco2, PRSC_con, NCI-H69 314758 AA521458 Hs.192738 ESTs 3.46 NCI-H23, NCI-H23, NCI-H520 334664 CH22_FGENES.418_15 3.45 NCI-H69, PRSC_log, PRSC_con 334661 CH22_FGENES.418_9 3.45 NCI-H69, PRSC_con, PRSC_log 330984 H38678 Hs.32766 H sapiens clone 24803 mRNA seq 3.44 OVCA-R, MCF7, PC3 333464 CH22_FGENES.160_1 3.44 NCI-H69, MB-MDA-231, MCF7 333580 CH22_FGENES.199_2 3.42 PRSC_con, NCI-H69, PRSC_log 313356 AI266254 Hs.132929 ESTs 3.42 RPWE-2, PRSC_con, NCI-H345 334518 CH22_FGENES.400_1 3.41 PRSC_log, PRSC_con, RPWE-2 333627 CH22_FGENES.225_2 3.4 HT29, BT474, BT474 309641 AW194230 Hs.253100 EST 3.4 HT29, MB-MDA-453, MCF7 338221 CH22_EM:AC005500.GENSCAN.246-10 3.4 NCI-H69, PRSC_log, NCI-H345 312993 AI392673 Hs.125230 ESTs 3.4 PRSC_log, NCI-H345, NCI-H345 318336 AI971806 Hs.164158 ESTs 3.38 OVCA-R, ES, CALU6 326218 CH.17_hs gi|5867226 3.38 NCI-H460, NCI-H69, NCI-H345 336231 CH22_FGENES.736_3 3.38 NCI-H69, NCI-H345, PRSC_log 307912 AI382224 EST singleton (not in UniGene) with exon 3.37 NCI-H345, PRSC_con, RPWE-2 336161 CH22FGENES.707_6 3.37 NCI-H69, NCI-H345, RPWE-2 300875 AW134756 Hs.192477 ESTs 3.37 RPWE-2, PRSC_log, PRSC_con 336593 CH22_FGENES.135_1 3.37 PRSC_con, NCI-H69, RPWE-2 310696 AI431620 Hs.160875 ESTs 3.36 HT29, OVCA-R, BT474 304745 AA577771 EST singleton (not in UniGene) with exon 3.36 NCI-H345, RPWE-2, PRSC_con 308911 AI860287 Hs.156110 Immunoglobulin kappa variable 1D-8 3.36 EB, DU145, CALU6 336347 CH22.FGENES.815_3 3.36 NCI-H69, PRSC_log, PRSC_con 334906 CH22_FGENES.452_21 3.33 Caco2, CALU6, MB-MDA-453 334548 CH22_FGENES.403_13 3.33 NCI-H345, PRSC_con, NCI-H69 336695 CH22_FGENES.48-4 3.32 NCI-H69, PRSC_log, PRSC_con 316684 AA807187 Hs.220783 ESTs; Weakly similar to WNT-1 PROTO-ONCO 3.31 DU145, ES, MB-MDA-231 315901 AI521558 Hs.179718 v-myb avian myeloblastosis viral oncogen 3.3 Caco2, LnCap, NCI-H69 320115 T93574 EST cluster (not in UniGene) 3.3 DU145, HT29, CALU6 307847 AI363993 Hs.157273 EST 3.3 NCI-H345, PRSC_con, PRSC_log 327899 CH.06_hs gi|5868156 3.28 BT474, MB-MDA-231, A549 304612 AA514207 EST singleton (not in UniGene) with exon 3.28 DU145, CALU6, LnCap 330021 CH.16_p2 gi|6671889 3.27 A549, HT29, EB 338132 CH22_EM:AC005500.GENSCAN.200-2 3.27 MB-MDA-231, CALU6, EB 323690 AA317497 Hs.188897 ESTs 3.27 RPWE-2, NCI-H345, MCF7 327362 CH.01_hs gi|6552412 3.26 NCI-H69, RPWE-2, PRSC_log 333488 CH22.FGENES.167_3 3.26 NCI-H69, NCI-H345, PRSC_log 334106 CH22_FGENES.330_5 3.26 NCI-H69, PRSC_con, PRSC_log 306990 AI129298 Hs.146491 EST; Weakly similar to FERRITIN HEAVY CH 3.26 NCI-H345, PRSC_log, PRSC_con 328420 CH.07_hs gi|5868411 3.26 NCI-H69, NCI-H345, PRSC_log 336214 CH22_FGENES.722_8 3.26 MCF7, ES, OVCA-R 330565 U51095 Hs.1545 caudal type homeo box transcription fact 3.25 EB, DU145, HT29 333879 CH22_FGENES.291_15 3.25 PRSC_con, PRSC_log, NCI-H69 300145 AI240850 Hs.232016 ESTs 3.25 NCI-H345, PRSC_con, PRSC_log 327581 CH.03_hs gi|5867825 3.25 EB, DU145, MB-MDA-453 308153 AI500429 Hs.1103 transforming growth factor; beta 1 3.24 MCF7, EB, EB 308337 AI608947 EST singleton (not in UniGene) with exon 3.24 PRSC_log, PRSC_con, NCI-H345 329406 CH.X_hs gi|6682547 3.23 DU145, HT29, MB-MDA-231 325482 CH.12_hs gi|5866957 3.23 NCI-H69, NCI-H345, PRSC_con 337544 CH22_FGENES.833-7 3.22 NCI-H69, NCI-H345, PRSC_con 337204 CH22_FGENES.595-1 3.22 NCI-H69, PRSC_con, PRSC_log 309451 AW105128 Hs.246687 EST 3.22 PRSC_con, RPWE-2, NCI-H345 337259 CH22_FGENES.649-3 3.2 PRSC_con, NCI-H345, NCI-H69 336489 CH22_FGENES.831_10 3.2 CALU6, MB-MDA-435s, Caco2 334804 CH22_FGENES.435_4 3.18 PRSC_log, PRSC_con, RPWE-2 335739 CH22_FGENES.601_10 3.18 NCI-H69, RPWE-2, PRSC_con 306264 AA935305 Hs.179779 ribosomal protein L37 3.17 LnCap, NCI-H69, EB 329386 CH.X_hs gi|6004484 3.17 RPWE-2, NCI-H345, PRSC_log 323479 AA278246 EST cluster (not in UniGene) 3.16 PRSC_con, NCI-H345, RPWE-2 304731 AA576085 EST singleton (not in UniGene) with exon 3.16 NCI-H69, LnCap, DU145 339419 CH22_DJ579N16.GENSCAN.11-11 3.15 NCI-H69, PRSC_log, RPWE-2 301202 AI536797 Hs.173155 ESTs 3.15 LnCap, NCI-H69, Caco2 333608 CH22_FGENES.216_3 3.15 NCI-H345, PRSC_con, PRSC_log 339193 CH22_FF113D11.GENSCAN.1-5 3.14 NCI-H69, NCI-H345, PRSC_con 310527 AW293404 Hs.211986 ESTs 3.14 PRSC_log, PRSC_con, RPWE-2 321146 AA707443 Hs.183983 ESTs 3.14 PRSC_con, NCI-H69, PRSC_log 333271 CH22_FGENES.121_2 3.13 NCI-H345, NCI-H69, RPWE-2 330280 CH.05_p2 gi|6671910 3.13 NCI-H69, NCI-H345, PRSC_log 309977 AW451663 EST singleton (not in UniGene) with exon 3.13 PRSC_con, PRSC_log, RPWE-2 307588 AI285535 EST singleton (not in UniGene) with exon 3.13 MB-MDA-231, BT474, BT474 330551 U39840 Hs.105440 hepatocyte nuclear factor 3; alpha 3.13 MB.MDA-453, LnCap, Caco2 314404 AW104203 Hs.157505 ESTs 3.13 DU145, EB, OVCA-R 334030 CH22_FGENES.320_2 3.13 NCI-H69, NCI-H345, PRSC_con 309108 AI925949 EST singleton (not in UniGene) with exon 3.13 BT474, MCF7, EB 317516 AI733250 Hs.192262 ESTs 3.12 OVCA-R, EB, MB-MDA-453 304161 H71886 EST singleton (not in UniGene) with exon 3.12 PRSC_con, NCI-H69, RPWE-2 334590 CH22_FGENES.407_13 3.12 NCI-H69, NCI-H345, PRSC_con 333408 CH22_FGENES.145_6 3.11 PRSC_log, RPWE-2, PRSC_con 330387 H14624 Hs.31386 ESTs; Highly similar to secreted apoptos 3.11 DU145, OVCA-R, PC3 332567 N23730 Hs.25647 v-fos FBJ murine osteosarcoma viral onco 3.11 EB, MB-MDA-453, MCF7 333682 CH22_FGENES.247_10 3.1 PRSC_con, PRSC_log, RPWE-2 323152 AI680562 Hs.246192 ESTs; Weakly similar to REGULATOR OF MIT 3.1 PC3, MB-MDA-453, DU145 311142 AI638441 Hs.195649 ESTs 3.1 PRSC_con, RPWE-2, PRSC_log 333441 CH22_FGENES.151_5 3.1 RPWE-2, NCI-H345, PRSC_log 326459 CH.19_hs gi|5867400 3.09 EB, CALU6, PC3 313493 AA910339 Hs.126868 ESTs 3.09 NCI-H345, PRSC_con, RPWE-2 339356 CH22_SA354I12.GENSCAN.31-1 3.08 NCI-H69, NCI-H345, PRSC_log 333629 CH22_FGENES.226_5 3.08 NCI-H69, NCI-H345, PRSC_log 304127 H42981 EST singleton (not in UniGene) with exon 3.07 LnCap, PRSC_con, DU145 325691 CH.14_hs gi|5867021 3.07 NCI-H345, PRSC_con, NCI-H69 333014 CH22_FGENES.61_6 3.07 PRSC_con, PRSC_log, NCI-H345 327379 CH.02_hs gi|5867795 3.07 PRSC_con, PRSC_log, NCI-H69 337816 CH22_EM:AC005500.GENSCAN.13-1 3.06 NCI-H69, PRSC_con, PRSC_log 337954 CH22_EM:AC005500.GENSCAN.96-3 3.06 PRSC_log, NCI-H69, NCI-H345 328109 CH.06_hs gi|5868020 3.05 HT29, BT474, MB-MDA-231 338527 CH22_EM:AC005500.GENSCAN.396-15 3.05 NCI-H69, NCI-H345, PRSC_con 320083 T87761 EST duster (not in UniGene) 3.05 BT474, MS-MDA-435s, MCF7 333486 CH22_FGENES.161_2 3.05 NCI-H345, RPWE-2, PRSC_log 334788 CH22.FGENES.432_13 3.04 EB, A549, CALU6 302681 X97550 EST 3.04 OVCA-R, EB, MB-MDA-453 336238 CH22_FGENES.743_3 3.03 NCI-H69, PRSC_log, PRSC_con 337606 CH22_C20H12.GENSCAN.17-2 3.02 HT29, BT474, MS-MDA-231 333545 CH22_FGENES.180_1 3.02 NCI-H69, NCI-H345, RPWE-2 309782 AW275156 Hs.156110 Immunoglobulin kappa variable 1D-8 3.02 PRSC_log, PRSC_con, RPWE-2 324277 AA429440 Hs.207285 ESTs 3.02 BT474, MB-MDA-231, HT29 321074 H38098 Hs.32756 ESTs 3.02 PC3, BT474, MB-MDA-231 337094 CH22_FGENES.465-19 3.01 PRSC_con, PRSC_log, RPWE-2 313913 AW391342 EST cluster (not in UniGene) 3 NCI-H345, RPWE-2, PRSC_log 329140 CH.X_hs gi|6017060 3 EB, DU145, PC3 335331 CH22.FGENES.535_4 3 MS-MDA-435s, HT29, BT474 334827 CH22_FGENES.437_9 2.99 CALU6, EB, DU145 326029 CH.17_hs gi|5867176 2.99 NCI-H345, RPWE-2, PRSC_con 303100 T09353 EST 2.99 MS-MDA-453, NCI-H345, RPWE-2 328768 CH.07_hs gi|6017031 2.99 NCI-H345, PRSC_con, NCI-H69 329392 CH.X_hs gi|6478815 2.98 NCI-H69, NCI-H345, PRSC_con 305168 AA663105 EST singleton (not in UniGene) with exon 2.98 LnCap, NCI-H345, MCF7 300992 AA601213 Hs.191798 ESTs 2.98 Caco2, HT29, NCI-358 334474 CH22_FGENES.394_5 2.98 NCI-H69, PRSC_con, RPWE-2 322647 AA007534 Hs.125062 ESTs 2.98 HT29, OVCA-R, A549 310620 AI341328 Hs.178953 ESTs 2.97 PRSC_con, RPWE-2, PRSC_log 328276 CH.07_hs gi|6004471 2.97 NCI-H345, NCI-H69, RPWE-2 331018 N26904 Hs.24048 ESTs; Weakly similar to FK506/rapamycin- 2.96 Caco2, NCI-H60, A549 321523 H78472 Hs.191325 ESTs; Weakly similar to cDNA EST yk414c9 2.96 PRSC_con, PRSC_log, NCI-H345 339280 CH22_BA354I12,GENSCAN.14-12 2.96 NCI-H69, PRSC_log, NCI-H345 305967 AA886428 EST singleton (not in UniGene) with exon 2.96 NCI-H520, NCI-358, MS-MDA-453 335755 CH22_FGENES.604_4 2.95 EB, A549, MB-MDA-453 323907 AL043098 Hs.165387 ESTs 2.95 PRSC_con, NCI-H345, PRSC_log 330370 CH.X_p2 gi|6580495 2.95 EB, DU145, MB-MDA-435s 334529 CH22_FGENES.402_9 2.94 EB, MCF7, DU145 339256 CH22_BA354I12.GENSCAN.7-11 2.94 NCI-H69, NCI-H345, PRSC_con 334783 CH22_FGENES.432_8 2.94 A549, Caco2, PC3 335266 CH22_FGENES.521_2 2.94 NCI-H69, PRSC_con, PRSC_con 323707 AA845957 Hs.128385 ESTs 2.94 NCI-H345, PRSC_con, PRSC_log 336199 CH22_FGENES.719_3 2.93 NCI-H69, NCI-H345, PRSC_log 338326 CH22_EM:AC005500.GENSCAN.308-2 2.93 NCI-H69, NCI-H345, NCI-358 333652 CH22_FGENES.239_1 2.93 PC3, OVCA-R, BT474 336479 CH22.FGENES.829_39 2.92 NCI-H69, PRSC_con, PRSC_log 336086 CH22_FGENES.688_15 2.92 PRSC_con, Caco2, CALU6 338516 CH22.EM:AC005500.GENSCAN.392-6 2.92 NCI-H69, NCI-H345, PRSC_con 320121 T93657 EST cluster (not in UrnGene) 2.92 EB, BT474, HT29 305782 AA844730 EST singleton (not in UniGene) with exon 2.92 MB-MDA-453, MCF7, DU145 339304 CH22_BA354I12.GENSCAN.20-16 2.91 PRSC_con, PRSC_log, NCI-H69 327472 CH.02_hs gi|5867775 2.91 PRSC_log, PRSC_con, RPWE-2 311458 AW139426 Hs.244718 ESTs 2.91 PRSC_con, PRSC_log, RPWE-2 338431 CH22_EM:AC005500.GENSCAN.351-4 2.9 BT474, MCF7, MB-MDA-453 339230 CH22_BA354I12.GENSCAN.1-6 2.89 NCI-H69, NCI-H345, PRSC_log 320588 NM_00365 EST cluster (not in UniGene) 2.89 OVCA-R, HT29, MB-MDA-231 304777 AA581692 Hs.2186 eukaryotic translation elongation factor 2.89 OVCA-R, EB, MCF7 337768 CH22_EM:AC000097.GENSCAN.119-6 2.88 NCI-H69, LnCap, DU145 319465 AA319115 Hs.191558 ESTs 2.88 NCI-H460, NCI-H520, NCI-358 319068 W93011 Hs.110155 ESTs 2.87 BT474, MB-MDA-453, MB-MDA-435s 330958 H08815 Hs.159824 EST 2.87 OVCA-R, PC3, A549 334215 CH22_FGENES.357_7 2.87 NCI-H69, PRSC_con, PRSC_log 333568 CH22_FGENES.185_1 2.87 PRSC_con, PRSC_log, NCI-H69 333142 CH22_FGENES.85_5 2.87 NCI-H69, HT29, HT29 330239 CH.05_p2 gi|6671857 2.87 MB-MDA-453, MB-MDA-453, EB 302120 R55140 Hs.31075 ESTs; Weakly similar to Weak similarity 2.87 CALU6, MB-MDA-435s, BT474 338679 CH22_EMAC005500.GENSCAN.470-1 2.86 NCI-H345, PRSC_log, PRSC_con 329041 CH.X_hs gi|5868564 2.86 LnCap, PRSC_con, RPWE-2 333541 CH22_FGENES.178_3 2.86 NCI-H69, NCI-H345, PRSC_con 337011 CH22_FGENES.427-6 2.86 NCI-H69, PRSC_log, PRSC_con 324031 AA375646 EST cluster (not in UniGene) 2.86 NCI-H345, PRSC_log, LnCap 331842 AA416586 Hs.98232 ESTs 2.86 DU145, OVCA-R, HT29 336599 CH22_FGENES.350_3 2.85 LnCap, NCI-H69, NCI-H345 337586 CH22_C20H12.GENSCAN.5-4 2.85 NCI-H345, NCI-H69, PRSC_con 336177 CH22_FGENES.712_2 2.85 NCI-H69, PRSC_log, RPWE-2 337522 CH22_FGENES.819-1 2.85 CALU6, OVCA-R, HT29 338598 CH22_EM:AC005500.GENSCAN.437-2 2.85 NCI-H69, PRSC_con, NCI-H345 309522 AW150044 Hs.252259 ribosomal protein S3 2.85 MB-MDA-453, MB-MDA-435s, MB-MDA-435s 336981 CH22_FGENES.397-7 2.85 NCI-H69, PRSC_con, PRSC_log 330286 CH.05_p2 gi|6671913 2.84 NCI-H345, PRSC_log, NCI-H69 333713 CH22_FGENES.251_2 2.84 RPWE-2, PRSC_con, NCI-H69 335068 CH22_FGENES.483_5 2.83 MB-MDA-231, NCI-H345, RPWE-2 305075 AA641288 Hs.181165 eukaryotic translation elongation factor 2.83 EB, LnCap, DU145 326380 CH.19_hs gi|5867327 2.82 NCI-H69, PRSC_con, PRSC_log 334970 CH22_FGENES.466_3 2.82 PRSC_con, NCI-H69, RPWE-2 337097 CH22_FGENES.471-1 2.82 NCI-H345, NCI-H69, PRSC_log 323676 AI702835 EST cluster (not in UniGene) 2.82 LnCap, A549, CALU6 333785 CH22.FGENES.274_4 2.82 OVCA-R, Caco2, MB-MDA-453 334175 CH22.FGENES.349_10 2.81 RPWE-2, BT474, MCF7 337865 CH22_EM:AC005500.GENSCAN.46-5 2.81 Caco2, NCI-H23, BT474 302585 AA083564 Hs.249220 H sapiens mRNA for hTbr2; complete cds 2.81 EB, DU145, MB-MDA-453 336623 CH22_FGENES.4-5 2.81 NCI-H345, PRSC_con, NCI-H69 332854 CH22.FGENES.22_1 2.8 RPWE-2, PRSC_log, PRSC_con 336978 CH22.FGENES.384-10 2.8 PRSC_con, NCI-H345, RPWE-2 326874 CH.20_hs gi|6682507 2.8 RPWE-2, NCI-H345, PRSC_log 315121 AA585011 Hs.105902 ESTs 2.8 NCI-H345, PRSC_log, RPWE-2 311185 AI638294 Hs.224665 ESTs 2.8 NCI-H69, NCI-H345, PRSC_log 334682 CH22_FGENES.419_4 2.8 NCI-H69, PRSC_log, RPWE-2 316845 AW418715 Hs.250388 ESTs 2.79 RPWE-2, NCI-H345, PRSC_log 331599 N74826 Hs.50535 ESTs 2.79 A549, MB-MDA-453, MB-MDA-435s 315681 AW022054 Hs.136591 ESTs 2.78 NCI-H460, MB-MDA-453, MCF7 313012 AI207390 Hs.143929 ESTs 2.78 DU145, MS-MDA-453, MCF7 313476 AA010267 EST cluster (not in UniGene) 2.78 NCI-H520, NCI-H460, HT29 327277 CH.01_hs gi|5867473 2.78 DU145, CALU6, EB 310981 AI494514 Hs.171380 ESTs 2.78 LnCap, RPWE-2, NCI-H460 335090 CH22.FGENES.490_1 2.77 NCI-H69, PRSC_log, PRSC_con 328581 CH.07.hs gi|6006033 2.77 HT29, MB-MDA-453, MCF7 333219 CH22_FGENES.104_11 2.77 NCI-H69, PRSC_log, NCI-H345 308311 AI581855 EST singleton (not in UniGene) with exon 2.77 MB-MDA-231, HT29, CALU6 329760 CH.14_p2 gi|6048280 2.77 CALU6, DU145, ES 303925 AW469999 Hs.258523 ESTs 2.77 NCI-H69, LnCap, MS-MDA-231 337628 CH22_C20H12.GENSCAN.28-31 2.77 NCI-H69, LnCap, MB-MDA-453 333520 CH22_FGENES.174_3 2.77 NCI-H69, NCI-H345, PRSC_con 303168 AA872479 Hs.197770 ESTs; Weakly similar to estrogen-respons 2.76 DU145, OVCA-R, MB-MDA-453 313451 AW138189 Hs.122672 ESTs 2.76 OVCA-R, EB, DU145 328474 CH.07_hs gi|5868446 2.76 NCI-H69, NCI-H345, RPWE-2 331988 AA477414 Hs.9242 purine-rich element binding protein B 2.76 MB-MDA-435s, A549, OVCA-R 306180 AA922503 EST singleton (not in UniGene) with exon 2.76 NCI-H69, DU145, LnCap 321071 AA013011 Hs.241502 Cdc42 effector protein 4 2.76 PRSC_log, PRSC_con, NCI-H345 302972 W73400 EST 2.76 NCI-H345, RPWE-2, NCI-H69 305185 AA663985 Hs.248038 major histocompatibility complex; class 2.75 DU145, A549, BT474 335998 CH22_FGENES.656_16 2.75 NCI-H69, PRSC_con, RPWE-2 319138 R11699 Hs.73818 ubiquinol-cytochrome c reductase hinge p 2.75 NCI-H345, NCI-H69, PRSC_con 336387 CH22_FGENES.822_7 2.75 PRSC_con, RPWE-2, PRSC_log 338054 CH22.EM:AC005500.GENSCAN.158-2 2.75 OVCA-R, EB, DU145 316041 AA719183 EST duster (not in UniGene) 2.74 DU145, MCF7, MB-MDA-453 336863 CH22_FGENES.297-4 2.74 MB-MDA-453, MCF7, OVCA-R 335975 CH22_FGENES.652_9 2.74 CALU6, EB, A549 302952 AF103179 EST 2.74 CALU6, MB.MDA-435s, BT474 326122 CH.17_hs gi|5867194 2.74 HT29, Caco2, PC3 337427 CH22_FGENES.761-4 2.74 RPWE-2, NCI-H89, PRSC_log 308063 AI469244 Hs.119252 tumor protein; translationally-controlle 2.74 NCI-358, NCI-H23, Caco2 325433 CH.12_hs gi|5866936 2.74 NCI-H345, PRSC_con, RPWE-2 316252 AI572633 Hs.190406 ESTs 2.74 OVCA-R, MCF7, A549 310837 AI418688 Hs.170301 ESTs 2.74 NCI-H345, PRSC_con, RPWE-2 313562 AW467335 Hs.257676 ESTs 2.74 HT29, MCF7, MB-MDA-231 335455 CH22_FGENES.562_15 2.74 NCI-H69, LnCap, PRSC_con 304792 AA583101 Hs.29797 ribosomal protein L10 2.73 EB, OVCA-R, MB-MDA-453 331979 AA469937 Hs.105322 EST 2.73 MCF7, BT474, NCI-H460 336198 CH22_PGENES.719_2 2.73 NCI-H69, PRSC_con, PRSC_log 314698 AI660452 Hs.187127 ESTs 2.73 MB-MDA-231, LnCap, BT474 307954 AI419692 EST singleton (not in UniGene) with exon 2.73 HT29, HT29, EB 318288 AI088590 Hs.134702 ESTs 2.73 PRSC_log, NCI-H345, PRSC_con 327833 CH.05_hs gi|5867968 2.73 BT474, PC3, MB-MDA-231 300221 AW449602 Hs.217953 ESTs; Highly similar to NK-TUMOR RECOGNI 2.73 NCI-H520, NCI-358, MB-MDA-453 326039 CH.17_hs gi|5867179 2.73 MB-MDA-453, EB, ES 318457 AI149678 Hs.143952 ESTs 2.72 PRSC_con, PRSC_log, NCI-H345 336753 CH22_FGENES.128-9 2.72 MB-MDA-435s, NCI-H520, MCF7 330086 CH.194_p2 gi|6015293 2.72 HT29, MB-MDA-453, MCF7 333566 CH22_FGENES.183_2 2.72 HT29, BT474, OVCA-R 339384 CH22_BA232E17.GENSCAN.3-22 2.71 NCI-H69, NCI-H345, PRSC_log 338668 CH22_EMAC005500.GENSCAN.465-1 2.71 NCI-H69, RPWE-2, PRSC_con 300798 AI382618 Hs.194813 ESTs 2.71 PRSC_con, NCI-H345, PRSC_log 303745 AI142379 EST 2.71 PRSC_log, PRSC_con, RPWE-2 305197 AA666301 EST singleton (not in UniGene) with exon 2.71 EB, NCI-H520, OVCA-R 338725 CH22_EM:AC005500.GENSCAN.499-1 2.7 OALU6, MB-MDA-453, PC3 307799 AI351112 EST singleton (not in UniGene) with exon 2.7 HT29, BT474, MCF7 309598 AW173642 Hs.250106 EST 2.69 NCI-358, NCI-H69, NCI-H23 302727 L10141 EST 2.69 OVCA-R, BT474, PC3 308544 AI695133 EST singleton (not in UniGene) with exon 2.69 HT29, CALU6, MB-MDA-435s 322877 AA079727 EST duster (not in UniGene) 2.69 NCI-H345, NCI-H69, PRSC_con 325695 CH.14_hs gi|6552446 2.69 NCI-H69, NCI-H460, NCI-H460 307728 AI335557 EST singleton (not in UniGene) with exon 2.68 NCI-H69, PRSC_log, NCI-358 302399 N79624 EST 2.68 NCI-H69, PRSC_con, NCI-H345 309343 AW028652 EST singleton (not in UniGene) with exon 2.68 HT29, MB-MDA-231, MB-MDA-231 339360 CH22_BA354I12.GENSCAN.32-2 2.68 NCI-H69, PRSC_log, PRSC_con 337821 CH22_EMAC005500.GENSCAN.13-11 2.68 PRSC_con, PRSC_log, PRSC_log 337338 CH22_FGENES.717-7 2.66 NCI-H69, PRSC_con, PRSC_log 334510 CH22_FGENES.398_8 2.68 NCI-H460, NCI-H23, NCI-358 300918 AA491286 Hs.128792 ESTs 2.68 MB-MDA-435s, CALU6, DU145 335536 CH22_FGENES.574_2 2.67 NCI-H69, NCI-H345, PRSC_log 335311 CH22_FGENES.532_4 2.67 MB-MDA-435s, Caco2, A549 338959 CH22_DJ32I10.GENSCAN.23-31 2.67 NCI-H345, PRSC_con, NCI-H69 339081 CH22_DA59H18.GENSCAN.37-10 2.67 NCI-H345, RPWE-2, NCI-H69 334068 CH22_FGENES.327_23 2.67 PRSC_con, RPWE-2, PRSC_log 338976 CH22_DAS9HI8.GENSCAN.1-3 2.66 PRSC_con, PRSC_log, RPWE-2 325524 CH.12_hs gi|5866981 2.66 NCI-H345, RPWE-2, PRSC_con 333069 CH22_FGENES.76_5 2.66 NCI-H69, NCI-H345, PRSC_con 336203 CH22_FGENES.719_7 2.66 OVCA-R, PC3, A549 333133 CH22_FGENES.83_9 2.66 HT29, OVCA-R, A549 304074 T77842 Hs.142528 ESTs 2.65 DU145, CALU6, EB 330919 AA224594 Hs.86941 ESTs 2.65 PRSC_con, RPWE-2, LnCap 333248 CH22_FGENES.115_5 2.65 NCI-H345, PRSC_con, MB-MDA-231 336665 CH22_FGENES.42-2 2.65 NCI-H69, PRSC_log, PRSC_con 315322 AA770599 EST cluster (not in UniGene) 2.65 A549, MB-MDA-453, MB-MDA-435s 307474 AI264023 EST singleton (not in UniGene) with exon 2.65 NCI-H69, NCI-H345, RPWE-2 320221 AL050020 Hs.127384 DKFZPS64C196 protein 2.65 MB-MDA-453, MCF7, HT29 301767 AW361892 EST 2.65 NCI-H345, PRSC_con, PRSC_log 327246 CH.01_hs gi|5867547 2.65 EB, OVCA-R, DU145 337403 CH22_FGENES.752-2 2.65 PRSC_con, PRSC_log, RPWE-2 328221 CH.06_hs gi|5868099 2.64 MCF7, MB-MDA-231, BT474 336759 CH22_FGENES.133-2 2.64 NCI-H69, PRSC_log, PRSC_con 327532 CH.02_hs gi|6469818 2.64 PC3, CALU6, A549 305621 AA789095 EST singleton (not in UniGene) with exon 2.64 HT29, MB-MDA-231, MB-MDA-453 322931 AA099329 Hs.151784 ESTs 2.64 PRSC_con, RPWE-2, NCI-H345 327278 CH.01_hs gi|5867473 2.64 EB, NCI-H460, NCI-H69 332235 N51413 Hs.109284 ESTs 2.64 DU145, EB, OVCA-R 332792 CH22_FGENES.3_2 2.63 HT29, Caco2, A549 312340 A1862668 Hs.176333 ESTs 2.63 NCI-358, NCI-358, HT29 337484 CH22_FGENES.795-8 2.63 NCI-H69, NCI-H345, PRSC_con 325783 CH.14_hs gi|6456780 2.63 EB, OVCA-R, PC3 303672 AW502380 Hs.210527 ESTs 2.63 PRSC_log, NCI-H345, NCI-H69 306009 AA894560 EST singleton (not in UniGene) with exon 2.63 HT29, MB-MDA-231, CALU6 308548 AI695484 EST singleton (not in UniGene) with exon 2.63 PC3, A549, NCI-358 337930 CH22_EM:AC005500.GENSCAN.81-3 2.62 PC3, OVCA-R, MCF7 327791 CH.05_hs gi|5867977 2.62 PRSC_log, PRSC_con, NCI-H345 330925 AA232678 Hs.87073 ESTs 2.62 OVCA-R, MCF7, LnCap 327259 CH.01_hs gi|5867454 2.62 NCI-H345, PRSC_con, RPWE-2 302150 AF061756 Hs.152531 heart and neural crest derivatives expre 2.61 OVCA-R, PC3, A549 304881 AA598501 Hs.195188 glyceraldehyde-3-phosphate dehydrogenase 2.61 MB-MDA-435s, NCI-H23, MCF7 335956 CH22_FGENES.647_3 2.61 DU145, PRSC_con, PC3 326506 CH.19_hs gi|5867435 2.61 RPWE-2, NCI-H460, NCI-358 335863 CH22_FGENES.629_8 2.61 PC3, HT29, NCI-358 334752 CH22_FGENES.428_1 2.61 PRSC_con, NCI-H69, PRSC_log 333288 CH22_FGENES.128_19 2.61 HT29, NCI-358, Caco2 306709 AI024215 Hs.131477 EST 2.61 MB-MDA-435s, MCF7, BT474 305816 AA854776 EST singleton (not in UniGene) with exon 2.6 MB-MDA-453, MCF7, MB-MDA-435s 327264 CH.01_hs gi|5867461 2.6 MB-MDA-435s, MB-MDA-435s, MB-MDA-453 310905 AW075527 Hs.252259 ribosomal protein S3 2.6 OVCA-R, EB, DU145 324492 AA479507 Hs.135179 ESTs 2.6 DU145, EB, OVCA-R 322649 AA526549 EST cluster (not in UniGene) 2.6 PRSC_con, RPWE-2, PRSC_log 329384 CH.X_hs gi|5868869 2.6 NCI-H69, NCI-H345, PRSC_con 321240 M62378 EST duster (not in UniGene) 2.6 BT474, CALU6, MB-MDA-231 302751 AA299576 Hs.156110 Immunoglobulin kappa variable 1D-8 2.59 MCF7, MB-MDA-453, OVCA-R 305841 AA860348 EST singleton (not in UniGene) with exon 2.59 NCI-H345, PRSC_log, PRSC_con 324180 AA402242 Hs.122799 ESTs 2.58 EB, PC3, HT29 334196 CH22_FGENES.353_4 2.58 NCI-H345, NCI-H69, PRSC_con 338451 CH22_EM:AC005500.GENSCAN.359-39 2.58 MB-MDA-435s, NCI-H23, MCF7 300333 AW297396 Hs.227052 ESTs 2.58 PRSC_con, PRSC_log, NCI-H69 305046 AA632201 EST singleton (not in UniGene) with exon 2.58 NCI-H460, MB-MDA-453, MB-MDA-435s 305648 AA807652 Hs.156110 Immunoglobulin kappa variable 1D-8 2.57 PRSC_con, RPWE-2, NCI-H345 301744 W22230 EST 2.57 PRSC_con, PRSC_log, NCI-H345 329182 CH.X_hs gi|6056331 2.57 PRSC_con, RPWE-2, NCI-H345 318178 AW137425 Hs.158401 ESTs 2.57 MB-MDA-231, PRSC_con, BT474 330057 CH.17_p2 gi|6478962 2.57 NCI-H345, RPWE-2, PRSC_con 326552 CH.19._hs gi|5867308 2.57 NCI-H345, PRSC_con, RPWE-2 311956 T67085 Hs.188484 ESTs 2.57 HT29, MB-MDA-453, NCI-H460 327185 CH.01_hs gi|6117805 2.57 CALU6, HT29, EB 302183 NM_00224 EST 2.57 MCF7, PC3, OVCA-R 327263 CH.01_hs gi|6525274 2.56 PRSC_con, NCI-H69, PRSC_log 339164 CH22.DA59H18.GENSCAN.69-4 2.56 NCI-H69, PRSC_con, NCI-H345 332763 AA063554 Hs.90959 ESTs 2.58 RPWE-2, NCI-H345, PRSC_con 330579 U67733 Hs.154437 phosphodiesterase 2A; cGMP-stimulated 2.55 HT29, CALU6, PC3 329948 CH.16_p2 gi|5540101 2.55 NCI-H460, MCF7, MB-MDA-453 300282 AW044305 Hs.236131 ESTs; Highly similar to homeodomain-inte 2.55 NCI-H460, NCI-H23, NCI-H23 335448 CH22_FGENES.562_5 2.55 MB-MDA-453, BT474, MCF7 330959 H09174 Hs.26484 HIRA-interacting protein 3 2.55 MB-MDA-453, HT29, MCF7 307262 AI202100 EST singleton (not in UniGene) with exon 2.55 MCF7, DU145, MB-MDA-435s 335806 CH22_FGENES.616_8 2.55 NCI-H345, NCI-H69, PRSC_con 335782 CH22_FGENES.609_4 2.55 Caco2, MB-MDA-453, MB-MDA-435s 301703 AW301478 EST 2.55 PC3, MCF7, MB-MDA-453 329018 CH.X_hs gi|6249620 2.54 NCI-H69, PRSC_log, PRSC_con 329870 CH.14_p2 gi|6706435 2.54 NCI-H23, NCI-H460, NCI-358 334504 CH22_FGENES.398_2 2.54 HT29, BT474, MB.MDA-231 304707 AA564846 EST singleton (not in UniGene) with exon 2.53 NCI-H520, EB, NCI-H460 329326 CH.X_hs gi|5868806 2.53 MB-MDA-231, NCI-H345, NCI-H69 334418 CH22_FGENES.384_5 2.53 NCI-H23, NCI-358, NCI-H460 338124 CH22_EM:AC005500.GENSCAN.196-2 2.53 NCI-H69, PRSC_con, PRSC_log 318423 AI362671 Hs.214491 ESTs 2.53 OVCA-R, EB, DU145 333006 CH22_FGENES.60_3 2.53 NCI-H69, PRSC_con, PRSC_log 333668 CH22_FGENES.245_2 2.53 NCI-H69, PRSC_log, PRSC_con 333567 CH22_FGENES.184_2 2.63 NCI-H69, NCI-H345, PRSC_con 309592 AW172384 EST singleton (not in UniGene) with exon 2.52 LnCap, NCI-H69, DU145 328989 CH.09_hs gi|5868535 2.52 MB-MDA-435s, OVCA-R, EB 326725 CH.20_hs gi|6552456 2.52 PRSC_con, NCI-H345, NCI-H69 302996 AF054863 EST 2.52 HT29, BT474, CALU6 335733 CH22_FGENES.601_3 2.52 NCI-H69, PRSC_log, NCI-H345 336000 CH22_FGENES.658_1 2.52 LnCap, OVCA-R, DU145 327774 CH.05_hs gi|5867964 2.52 DU145, CALU6, HT29 328557 CH.07_hs gi|5868489 2.52 MB-MDA-453, MB-MDA-435s, MCF7 328228 CH.06_hs gi|5868105 2.52 NCI-H69, NCI-H345, PRSC_con 328305 CH.07_hs gi|6004478 2.52 NCI-H69, NCI-H460, PRSC_log 334010 CH22_FGENES.313_1 2.51 NCI-H69, PRSC_log, PRSC_con 339033 CH22_DA59H18.GENSCAN.26-1 2.51 NCI-H69, NCI-H345, PRSC_con 335340 CH22_FGENES.535_17 2.51 NCI-H69, PRSC_con, PRSC_log 300156 AI245582 Hs.233395 ESTs 2.51 PRSC_con, PRSC_log, NCI-H345 305880 AA866065 Hs.156110 Immunoglobulin kappa variable 1D-8 2.5 EB, OVCA-R, DU145 310841 AI968009 Hs.232024 ESTs 2.5 LnCap, NCI-358, CALU6 336908 CH22_FGENES.343-2 2.5 NCI-H345, RPWE-2, PRSC_log 304674 AA541735 EST singleton (not in UniGene) with exon 2.5 RPWE-2, NCI-H69, MCF7 314521 AW503939 Hs.107149 ESTs; Weakly similar to PTB-ASSOCIATED S 2.5 NCI-H460, EB, Caco2 307592 AI285739 EST singleton (not in UniGene) with exon 2.5 PRSC_con, NCI-H345, PRSC_log 331476 N26190 Hs.43768 ESTs 2.5 NCI-H345, NCI-H69, PRSC_con 325803 CH.14_hs gi|6552451 2.5 NCI-H345, RPWE-2, PRSC_con 306549 AA993796 EST singleton (not in UniGene) with exon 2.49 A549, OVCA-R, CALU6 304833 AA586504 EST singleton (not in UniGene) with exon 2.49 MCF7, DU145, LnCap 336333 CH22_FGENES.813.1 2.49 NCI-H345, PRSC_con, PRSC_log 332320 T71134 Hs.100551 EST 2.49 NCI-H345, LnCap, RPWE-2 328236 CH.06_hs gi|5868117 2.49 PRSC_con, NCI-H345, PRSC_log 317335 AI656979 Hs.130210 ESTs 2.49 MCF7, MB-MDA-453, PC3 339188 CH22_DA59H18.GENSCAN.72-16 2.48 NCI-H69, PRSC_con, PRSC_log 334235 CH22_FGENES.361_19 2.48 NCI-H520, MB-MDA-453, A549 301214 AW450950 Hs.157034 ESTs; Weakly similar to Unknown [H.sapie 2.48 HT29, A549, A549 332843 CH22_FGENES.19_1 2.48 DU145, CALU6, EB 337431 CH22_FGENES.763-7 2.48 PRSC_con, RPWE-2, NCI-H69 336757 CH22_FGENES.131-1 2.48 NCI-H69, PRSC_log, PRSC_con 305403 AA723748 EST singleton (not in UniGene) with exon 2.48 NCI-H23, DU145, OVCA-R 330065 CH.19_p2 gi|6165044 2.48 PRSC_con, PRSC_log, NCI-H69 309245 AI972447 EST singleton (not in UniGene) with exon 2.48 MB-MDA-231, NCI-H69, HT29 328876 CH.07_hs gi|6525286 2.47 MB-MDA-231, CALU6, PC3 333944 CH22_FGENES.302_2 2.47 NCI-H69, RPWE-2, PRSC_log 328504 CH.07_hs gi|5868471 2.47 LnCap, MB-MDA-453, MB-MDA-435s 336120 CH22_EM:AC005500.GENSCAN.195-1 2.47 MB-MDA-231, NCI-H69, PRSC_con 306710 AI024221 EST singleton (not in UniGene) with exon 2.47 OVCA-R, EB, LnCap 305064 AA636012 EST singleton (not in UniGene) with exon 2.47 NCI-H69, RPWE-2, PRSC_con 329995 CH.16_p2 gi|4567166 2.47 OVCA-R, DU145, MB-MDA-453 315694 AI821743 Hs.168418 ESTs; Moderately similar to !!!! ALU SUB 2.46 EB, A549, LnCap 331004 H64622 Hs.32748 ESTs 2.46 EB, MCF7, MB-MDA-435s 305259 AA679225 EST singleton (not in UniGene) with exon 2.46 PRSC_con, NCI-H345, RPWE-2 304576 AA496563 EST singleton (not in UniGene) with exon 2.46 PRSC_con, RPWE-2, PRSC_log 318887 R60487 Hs.21065 ESTs 2.46 NCI-H345, Caco2, Caco2 308954 AI868958 EST singleton (not in UniGene) with exon 2.46 PRSC_con, PRSC_log, RPWE-2 301140 AI807692 Hs.207128 ESTs 2.46 OVCA-R, MB-MDA-231, HT29 322085 AA088500 Hs.170298 ESTs 2.46 PRSC_log, PRSC_con, NCI-H345 339130 CH22_DA59H18.GENSCAN.56-3 2.46 NCI-H345, PRSC_con, RPWE-2 337612 CH22_C20H12.GENSCAN.22-5 2.46 EB, A549, Caco2 313765 AW206181 Hs.185981 ESTs; Weakly similar to gag [H.sapiens] 2.45 RPWE-2, PRSC_log, PRSC_con 311665 AW294254 Hs.223742 ESTs 2.45 PRSC_log, RPWE-2, PRSC_con 328620 CH.07.hs gi|5868241 2.45 MB-MDA-453, MCF7, MB-MDA-435s 305361 AA708902 EST singleton (not in UniGene) with exon 2.45 HT29, MB-MDA-435s, A549 336243 CH22_FGENES.746_1 2.44 OVCA-R, MB-MDA-453, MB-MDA-435s 320299 H08323 Hs.177181 ESTs 2.44 PRSC_con, RPWE-2, NCI-H345 302535 H48676 EST 2.44 MB-MDA-453, EB, DU145 333465 CH22_FGENES.160_2 2.44 NCI-H69, PRSC_con, PRSC_log 334109 CH22_FGENES.330_8 2.44 NCI-H69, NCI-H345, PRSC_log 301749 F12998 Hs.90790 ESTs 2.44 NCI-H345, RPWE-2, PRSC_log 324575 AW502257 EST cluster (not in UniGene) 2.44 NCI-H345, PRSC_con, RPWE-2 337114 CH22_FGENES.494-17 2.44 NCI-H69, PRSC_log, PRSC_con 336087 CH22_FGENES.688_16 2.44 PRSC_con, Caco2, PRSC_log 315678 AI657119 Hs.120036 ESTs 2.44 NCI-358, PC3, NCI-H23 333258 CH22.FGENES.118_6 2.44 MB-MDA-231, HT29, CALU6 303798 V00505 Hs.36977 hemoglobin; delta 2.44 MB-MDA-435s, MCF7, MB-MDA-453 309759 AW268822 EST singleton (not in UniGene) with exon 2.44 MB-MDA-453, EB, MCF7 318946 AI122843 EST cluster (not in UniGene) 2.44 PC3, OVCA-R, DU145 321986 AL133656 EST cluster (not in UniGene) 2.44 DU145, CALU6, CALU6 336151 CH22_EM:AC005500.GENSCAN.207-5 2.44 PRSC_con, PRSC_log, RPWE-2 327056 CH.21_hs gi|6531965 2.44 PRSC_con, NCI-H345, RPWE-2 309605 AW182800 EST singleton (not in UniGene) with exon 2.43 NCI-358, NCI-H23, NCI-H520 335783 CH22_FGENES.610_3 2.43 PRSC_con, PRSC_log, NCI-H345 325790 CH.14_hs gi|6381957 2.43 MB-MDA-435s, MB-MDA-453, MB-MDA-453 339342 CH22_BA354I12, GENSCAN.27-10 2.43 BT474, MB-MDA-231, MB-MDA-453 335777 CH22_FGENES.607_13 2.43 DU145, EB, BT474 309972 AW450350 Hs.257283 ESTs 2.43 MCF7, MB-MDA-453, OVCA-R 308718 AI798009 EST singleton (not in UniGene) with exon 2.43 NCI-H345, PRSC_con, PRSC_log 338087 CH22_EM:AC005500.GENSCAN.174-16 2.43 DU145, PC3, CALU6 306930 AI124518 EST singleton (not in UniGene) with exon 2.43 NCI-H69, MCF7, BT474 319032 AW409728 Hs.80449 ESTs; Weakly similar to cytoplasmic dyne 2.43 RPWE-2, A549, NCI-H69 304330 AA157834 EST singleton (not in UniGene) with exon 2.43 MB-MDA-453, PC3, OVCA-R 320636 R54766 Hs.101120 ESTs 2.43 MCF7, MB-MDA-435s, MB-MDA-453 335281 CH22_FGENES.524_4 2.43 PC3, LnCap, A549 317431 AI675790 Hs.132453 ESTs 2.43 NCI-H345, RPWE-2, PRSC_log 306511 AA988891 EST singleton (not in UniGene) with exon 2.43 OVCA-R, EB, DU145 333298 CH22_FGENES.133_4 2.43 EB, DU145, PC3 328436 CH.07_hs gi|5868417 2.43 EB, LnCap, A549 333420 CH22_FGENES.146_11 2.43 NCI-H345, NCI-H69, PRSC_log 338113 CH22_EM:AC005500.GENSCAN.188-13 2.42 DU145, EB, CALU6 335188 CH22_FGENES.507_3 2.42 EB, A549, BT474 329164 CH.X_hs gi|5868691 2.42 RPWE-2, PRSC_con, PRSC_log 336316 CH22_FGENES.799_11 2.42 MB-MDA-435s, MCF7, NCI-H69 310831 AI927594 Hs.161142 ESTs 2.42 NCI-H345, PRSC_con, PRSC_log 327334 CH.01_hs gi|5902477 2.42 MB-MDA-453, MB-MDA-435s, MCF7 334017 CH22_FGENES.315_2 2.42 PRSC_con, PRSC_log, RPWE-2 308138 AI494446 EST singleton (not in UniGene) with exon 2.42 DU145, LnCap, EB 333074 CH22_FGENES.76_10 2.42 NCI-H69, RPWE-2, PRSC_log 306548 AA993109 EST singleton (not in UniGene) with exon 2.42 HT29, CALU6, LnCap 336516 CH22_FGENES.836_1 2.42 NCI-H69, PRSC_con, PRSC_log 306791 AI042387 EST singleton (not in UniGene) with exon 2.42 CALU6, DU145, EB 329411 CH.X_hs gi|6682549 2.42 OVCA-R, EB, LnCap 308659 AI750091 EST singleton (not in UniGene) with exon 2.41 EB, DU145, CALU6 313504 AI190405 Hs.143127 ESTs 2.41 DU145, EB, CALU6 326073 CH.17_hs gi|6682495 2.41 DU145, A549, MB-MDA-435s 334047 CH22_FGENES.326_5 2.41 PRSC_con, PRSC_log, NCI-H345 325464 CH.12_hs gi|5866947 2.41 NCI-358, NCI-H23, NCI-H460 334764 CH22_FGENES.428_13 2.41 NCI-H69, NCI-H345, RPWE-2 312737 AI033500 Hs.132895 ESTs 2.41 OVCA-R, DU145, CALU6 306591 AI000248 EST singleton (not in UniGene) with exon 2.41 MB-MDA-231, MCF7, DU145 333582 CH22_FGENES.201_2 2.41 NCI-H69, PRSC_con, PRSC_log 337843 CH22_EM:AC005500.GENSCAN.30-8 2.4 EB, LnCap, A549 335284 CH22_FGENES.526_6 2.4 NCI-H69, NCI-H345, PRSC_log 305134 AA653159 EST singleton (not in UniGene) with exon 2.4 DU145, HT29, MB-MDA-453 335527 CH22_FGENES.572_7 2.4 DU145, OVCA-R, EB 336795 CH22_FGENES.176-5 2.4 NCI-H69, NCI-H345, PRSC_log 303144 AF202889 EST 2.4 PRSC_con, PRSC_log, NCI-H69 334948 CH22_FGENES.465_15 2.4 PRSC_con, PRSC_log, RPWE-2 328860 CH.07_hs gi|6381928 2.4 PRSC_con, PRSC_log, NCI-H345 322929 AI365585 Hs.148246 ESTs 2.4 NCI-H460, A549, HT29 333561 CH22_FGENES.180_18 2.4 OVCA-R, EB, DU145 338239 CH22_EM:AC005500.GENSCAN.264-5 2.4 NCI-H69, NCI-H345, PRSC_con 323670 AL040411 Hs.161763 ESTs; Weakly similar to KIAA0738 protein 2.4 DU145, MB-MDA-453, EB 305903 AA873085 EST singleton (not in UniGene) with exon 2.4 MCF7, A549, NCI-H520 312573 AW297673 Hs.190526 ESTs 2.4 LnCap, NCI-H460, NCI-H23 334470 CH22_FGENES.394_1 2.4 NCI-H520, HT29, NCI-H23 333272 CH22_FGENES.122_1 2.39 NCI-H345, PRSC_con, RPWE-2 304010 AW518383 Hs.177592 ribosomal protein; large; P1 2.39 DU145, CALU6, EB 337316 CH22_FGENES.692-1 2.39 MCF7, BT474, OVCA-R 316769 AI914939 Hs.212184 ESTs 2.39 PRSC_con, NCI-H345, RPWE-2 336280 CH22_FGENES.763_4 2.39 NCI-H345, PRSC_log, PRSC_con 331223 T98872 Hs.194181 ESTs 2.39 DU145, HT29, PC3 337172 CH22_FGENES.565-2 2.39 EB, OVCA-R, DU145 300625 AI671992 Hs.143631 ESTs; Weakly similar to WASP-family prot 2.39 EB, NCI-H520, LnCap 337092 CH22_FGENES.465-12 2.39 PRSC_con, PRSC_log, NCI-H69 334528 CH22_FGENES.402_8 2.39 NCI-H345, PRSC_con, NCI-H69 338411 CH22_EM:AC005500.GENSCAN.341-7 2.39 NCI-H345, NCI-H69, PRSC_con 331344 AA357927 Hs.70208 ESTs 2.39 PC3, EB, A549 334044 CH22.FGENES.323_2 2.38 MB-MDA-231, MCF7, LnCap 333918 CH22_FGENES.296_7 2.38 RPWE-2, NCI-H345, EB 317168 AI042614 Hs.125910 ESTs 2.38 NCI-H345, PRSC_con, RPWE-2 333424 CH22_FGENES.147_4 2.38 DU145, MCF7, OVCA-R 317779 AW450515 Hs.128361 ESTs 2.38 EB, DU145, OVCA-R 315142 AI380577 Hs.190219 ESTs 2.38 OVCA-R, EB, CALU6 310471 AW270515 Hs.149596 ESTs 2.38 NCI-H460, NCI-H23, NCI-H23 325049 AW410339 Hs.256310 ESTs; Weakly similar to centaurin beta2 2.38 PRSC_con, RPWE-2, NCI-H345 305234 AA670431 EST singleton (not in UniGene) with exon 2.38 MB-MDA-453, MB-MDA-231, A549 337760 CH22_EM:AC000097.GENSCAN.116-8 2.38 PRSC_con, PRSC_log, RPWE-2 311502 AW204360 Hs.208662 ESTs 2.38 NCI-H345, NCI-H69, LnCap 337548 CH22_FGENES.844-5 2.38 MB-MDA-453, MCF7, CALU6 326981 CH.21_hs gi|6588016 2.38 NCI-H348, NCI-H69, PRSC_con 309600 AW182066 EST singleton (not in UniGene) with exon 2.37 RPWE-2, NCI-358, NCI-H69 328936 CH.08_hs gi|5868500 2.37 OVCA-R, MB-MDA-453, CALU6 327937 CH.06_hs gi|5868192 2.37 BT474, EB, OVCA-R 328282 CH.07_hs gi|5868353 2.37 DU145, CALU6, CALU6 303607 AL046388 Hs.208206 ESTs; Weakly similar to Naf1 alpha prote 2.37 LnCap, PRSC_log, NCI-H345 304227 N94974 Hs.75344 ribosomal protein S4; X-linked 2.37 EB, PC3, OVCA-R 314101 AW452279 Hs.257542 ESTs 2.37 OVCA-R, CALU6, CALU6 325026 AI671168 Hs.12285 ESTs 2.37 NCI-H345, PRSC_con, PRSC_log 315015 AI659989 Hs.132625 ESTs 2.37 MB-MDA-453, MB-MDA-231, LnCap 328662 CH.07_hs gi|6004473 2.37 NCI-H345, RPWE-2, PRSC_con 305867 AA864572 EST singleton (not in UniGene) with exon 2.37 MCF7, MB-MDA-453, MB-MDA-231 333296 CH22_FGENES.132_3 2.37 EB, PC3, CALU6 331070 R01116 Hs.182059 ESTs 2.36 OVCA-R, MB-MDA-453, A549 333698 CH22_FGENES.250_12 2.36 HT29, OVCA-R, Caco2 316423 AA758756 Hs.121380 ESTs 2.36 HT29, MCF7, MB-MDA-435s 323189 AL121194 Hs.120589 ESTs 2.36 PC3, NCI-H460, DU145 318889 Z43296 Hs.18720 programmed cell death 8 (apoptosis-induc 2.36 OVCA-R, A549, MB-MDA-453 334237 CH22_FGENES.362_1 2.36 NCI-H345, NCI-H69, LnCap 315931 AI700148 Hs.117328 ESTs 2.36 MCF7, NCI-H345, DU145 326884 CH.20_hs gi|668251 1 2.36 A549, EB, PC3 333132 CH22_FGENES.83_8 2.36 NCI-H69, HT29, EB 306574 AA995719 Hs.76067 heat shock 27 kD protein 1 2.36 RPWE-2, PRSC_log, PRSC_con 324416 AI669524 Hs.194115 ESTs 2.36 NCI-H345, RPWE-2, PRSC_con 329496 CH.10_p2 gi|3983518 2.35 HT29, MCF7, MB-MDA-231 320994 H22381 EST cluster (not in UniGene) 2.35 NCI-H23, A549, CALU6 320481 AA461139 Hs.24372 ESTs; Weakly similar to dJ207H1.1 [H.sap 2.35 PRSC_con, RPWE-2, PRSC_log 309958 AW444488 EST singleton (not in UniGene) with exon 2.35 NCI-H345, PRSC_con, PRSC_log 327009 CH.21_hs gi|5867664 2.35 HT29, BT474, MCF7 309594 AW172821 Hs.181165 eukaryotic translation elongation factor 2.35 HT29, DU145, EB 335468 CH22_FGENES.567_4 2.35 NCI-H69, PRSC_con, NCI-H345 304269 AA069029 EST singleton (not in UniGene) with exon 2.35 PRSC_con, PRSC_log, RPWE-2 305877 AA865649 EST singleton (not in UniGene) with exon 2.35 A549, MCF7, OVCA-R 305700 AA815428 EST singleton (not in UniGene) with exon 2.35 PRSC_con, NCI-H345, PRSC_log 326423 CH.19_hs gi|5867369 2.34 PC3, MCF7, LnCap 334560 CH22_FGENES.404_3 2.34 HT29, NCI-H460, MB-MDA-435s 337100 CH22_FGENES.472-3 2.34 PRSC_log, PRSC_con, RPWE-2 301505 AW014374 Hs.144849 ESTs 2.34 CALU6, MB-MDA-231, DU145 312142 AW298359 Hs.221069 ESTs 2.34 PRSC_con, RPWE-2, PRSC_log 305787 AA845035 EST singleton (not in UniGene) with exon 2.34 NCI-H23, NCI-H520, NCI-H460 338686 CH22_EM:AC005500.GENSCAN.472-5 2.33 BT474, MB-MDA-231, MB-MDA-453 331977 AA465207 Hs.125887 ESTs 2.33 OVCA-R, A549, MB-MDA-435s 314687 M79114 Hs.135177 ESTs 2.33 NCI-H69, PRSC_con, NCI-H345 336089 CH22_FGENES.688_18 2.33 PRSC_con, Caco2, PRSC_log 338952 CH22_DJ32110.GENSCAN.23-22 2.33 PC3, OVCA-R, HT29 334612 CH22_FGENES.411_11 2.33 OVCA-R, MB-MDA-453, EB 338223 CH22_EM:AC005500.GENSCAN.250-10 2.33 DU145, MB-MDA-453, MCF7 327845 CH.05_hs gi|6531962 2.32 OVCA-R, MB-MDA-453, PC3 308187 AI538108 Hs.156110 Immunoglobulin kappa variable 10-8 2.32 NCI-H69, NCI-358, PRSC_con 317767 AW294164 Hs.128340 ESTs; Weakly similar to Cdc42 GTPase-act 2.32 BT474, CALU6, MB-MDA-231 330408 L10343 Hs.112341 protease inhibitor 3; skin-derived (SKAL 2.32 PC3, Caco2, HT29 319003 R17712 EST cluster (not in UniGene) 2.32 MCF7, PC3, MB-MDA-453 323022 AI066733 Hs.133885 ESTs 2.32 CALU6, MB-MDA-231, DU145 303148 R73167 Hs.127317 ESTs; Weakly similar to CYTOCHROME P450 2.32 NCI-H345, PRSC_con, RPWE-2 303215 AW250314 EST 2.32 NCI-H345, PRSC_con, PRSC_log 318891 H10477 Hs.196208 ESTs; Weakly similar to !!!! ALU SUBFAMI 2.32 NCI-H69, LnCap, NCI-H345 336653 CH22_FGENES.33-4 2.32 DU145, EB, LnCap 333329 CH22_FGENES.138_22 2.32 DU145, BT474, MB-MDA-231 301980 U69962 Hs.121498 potassium voltage-gated channel; Shab-re 2.31 NCI-H345, MB-MDA-231, LnCap 336968 CH22_FGENES.375-28 2.31 HT29, BT474, EB 308539 AI694191 EST singleton (not in UniGene) with exon 2.31 NCI-H345, NCI-H69, PRSC_log 326417 CH.19_hs gi|5867362 2.31 HT29, MCF7, BT474 328861 CH.07_hs gi|6381923 2.31 NCI-H520, NCI-H460, NCI-H23 329254 CH.X_hs gi|5868733 2.31 RPWE-2, NCI-H345, PRSC_con 303075 W88779 Hs.59125 ESTs 2.3 DU145, OVCA-R, EB 335131 CH22_FGENES.497_15 2.3 NCI-H69, NCI-H345, PRSC_log 303129 AA308334 Hs.172210 MUF1 protein 2.3 LnCap, DU145, HT29 327067 CH.21_hs gi|6531965 2.3 NCI-H345, NCI-H69, MB-MDA-435s 324064 AW137650 EST cluster (not in UniGene) 2.3 DU145, HT29, EB 325965 CH.16_hs gi|5887147 2.3 NCI-H69, NCI-H345, RPWE-2 334525 CH22_FGENES.402_4 2.3 NCI-H345, PRSC_con, NCI-H69 336654 CH22_FGENES.34-2 2.3 BT474, PC3, ME-MDA-453 302348 AF100779 Hs.194680 WNT1 inducible signaling pathway protein 2.3 LnCap, CALU6, DU145 309275 AI989570 EST singleton (not in UniGene) with exon 2.3 NCI-H460, NCI-H23, NCI-H520 329246 CH.X_hs gi|5868732 2.3 NCI-H69, NCI-H345, PRSC_log 305557 AA774834 EST singleton (not in UniGene) with exon 2.3 CALU6, CALU6, MCF7 322907 AA084941 EST cluster (not in UniGene) 2.3 MB-MDA-231, CALU6, EB 318683 AI703241 Hs.202653 ESTs; Weakly similar to Xin [M.musculus] 2.29 NCI-H345, PRSC_con, RPWE-2 309233 AI971416 EST singleton (not in UniGene) with exon 2.29 CALU6, OVCA-R, EB 308913 AI860692 Hs.119122 ribosomal protein L13a 2.29 MB-MDA-435s, MCF7, HT29 335827 CH22_FGENES.620_1 2.29 PRSC_con, PRSC_log, RPWE-2 334066 CH22_FGENES.327_21 2.29 PRSC_con, PRSC_log, NCI-H345 302656 AW293005 Hs.220905 ESTs 2.29 NCI-H23, Caco2, CALU6 308974 AI872290 Hs.140 immunoglobulin gamma 3 (Gm marker) 2.29 CALU6, A549, NCI-H69 333607 CH22_FGENES.216_2 2.29 OVCA-R, MCF7, A549 335174 CH22_FGENES.504_4 2.29 HT29, A549, MB-MDA-453 332028 AA489680 Hs.134406 ESTs; Weakly similar to Dim1p homolog [H 2.29 EB, A549, DU145 336417 CH22_FGENES.823_39 2.29 NCI-H69, NCI-H345, PRSC_log 323426 AA251401 EST cluster (not in UniGene) 2.29 HT29, MB-MDA-231, BT474 336618 CH22_FGENES.2-1 2.29 NCI-358, NCI-H460, NCI-H69 310017 AI188739 Hs.148488 ESTs 2.29 NCI-H345, PRSC_log, PRSC_con 334055 CH22_FGENES.327_6 2.28 DU145, OVCA-R, MB-MDA-453 337168 CH22_FGENES.562-28 2.28 NCI-H69, PRSC_log, NCI-H345 329824 CH.14_p2 gi|6630758 2.28 NCI-H23, CALU6, RPWE-2 333891 CH22_FGENES.292_13 2.28 NCI-H69, MB-MDA-231, RPWE-2 339127 CH22_DAS9H18.GENSCAN.55-1 2.28 PRSC_con, NCI-H345, RPWE-2 305686 AA812726 EST singleton (not in UniGene) with exon 2.28 NCI-H520, NCI-H23, NCI-H460 329782 CH.14_p2 gi|5912597 2.28 NCI-H69, NCI-H345, PRSC_log 311059 AI810001 Hs.175346 ESTs 2.28 MCF7, BT474, MB-MDA-435s 336934 CH22_FGENES.351-1 2.28 BT474, HT29, MB-MDA-435s 314893 AA761093 EST cluster (not in UniGene) 2.28 OVCA-R, HT29, DU145 331596 N72574 Hs.50220 ESTs 2.28 A549, MCF7, NCI-358 330729 AA258559 Hs.3736 ESTs; Weakly similar to DELTA-LIKE PROTE 2.28 MB-MDA-231, CALU6, MCF7 338285 CH22_EM:AC005500.GENSCAN.293-3 2.27 NCI-H69, PRSC_log, PRSC_con 300154 AI245127 Hs.179331 ESTs 2.27 NCI-H23, NCI-H520, NCI-358 306383 AA969078 Hs.183698 ribosomal protein L29 2.27 RPWE-2, NCI-H345, PRSC_log 309005 AI884454 EST singleton (not in UniGene) with exon 2.27 A549, MCF7, BT474 332995 CH22_FGENES.58_2 2.27 RPWE-2, NCI-H345, PRSC_log 337426 CH22_FGENES.761-3 2.27 DU145, EB, CALU6 337778 CH22_EM:AC000097.GENSCAN.119-20 2.27 NCI-H69, PRSC_con, PRSC_log 329705 CH.14_p2 gi|6065790 2.27 PRSC_con, PRSC_log, RPWE-2 335971 CH22_FGENES.652_4 2.27 PRSC_log, MB-MDA-231, NCI-H23 315862 AI075848 Hs.133996 ESTs 2.27 HT29, MB-MDA-435s, OVCA-R 316466 AI911204 Hs.126365 ESTs 2.27 NCI-8460, NCI-358, BT474 334430 CH22_FGENES.385_3 2.27 NCI-H345, NCI-H69, PRSC_con 331941 AA452257 Hs.99272 ESTs 2.26 PRSC_con, LnCap, PRSC_log 301230 AW269804 Hs.153019 ESTs 2.26 NCI-H345, PRSC_log, NCI-H520 317394 AI935024 Hs.190518 ESTs 2.26 NCI-H345, PRSC_con, PRSC_log 306220 AA928363 EST singleton (not in UniGene) with exon 2.26 NCI-H345, PRSC_con, PRSC_log 304134 H54627 EST singleton (not in UniGene) with exon 2.26 DU145, CALU6, PC3 335421 CH22_FGENES.55_1 2.26 NCI-H69, PRSC_con, PRSC_log 305260 AA679280 Hs.156110 Immunoglobulin kappa variable 10-8 2.26 NCI-H345, NCI-H69, PRSC_con 303592 AA421129 EST 2.26 CALU6, OVCA-R, DU145 317982 AI004985 Hs.130607 ESTs 2.26 PC3, MB-MDA-435s, A549 325304 CH11_hs gi|5866910 2.26 MCF7, CALU6, A549 334118 CH22_FGENES.330_19 2.26 PRSC_con, NCI-H69, PRSC_log 335687 CH22_FGENES.596_2 2.26 A549, CALU6, LnCap 334035 CH22_FGENES.322.3 2.26 NCI-H345, PRSC_con, RPWE-2 305454 AA738413 EST singleton (not in UniGene) with exon 2.25 EB, HT29, CALU6 335902 CH22_FGENES.635_10 2.25 EB, DU145, HT29 339215 CH22_FF113D11.GENSCAN.6-10 2.25 PRSC_con, PRSC_log, RPWE-2 328810 CH.07_hs gi|5868327 2.25 PC3, OVCA-R, MB-MDA-453 337396 CH22_FGENES.749-1 2.25 EB, A549, DU145 336808 CH22_FGENES.205-3 2.25 NCI-H345, NCI-H69, PRSC_con 305808 AA853958 EST singleton (not in UniGene) with exon 2.24 MB-MDA-453, DU145, EB 333571 CH22_FGENES.188_2 2.24 MCF7, MB-MDA-453, PC3 323023 AA225188 Hs.258539 ESTs 2.24 EB, DU145, CALU6 334626 CH22_FGENES.416_2 2.24 NCI-H69, NCI-H345, PRSC_log 333593 CH22_FGENES.210_2 2.24 NCI-H69, NCI-H345, PRSC_con 326708 CH.20_hs gi|5867593 2.24 NCI-H460, NCI-H23, NCI-H520 314502 AI041717 Hs.132141 ESTs 2.23 NCI-H345, RPWE-2, PRSC_con 309181 AI951727 EST singleton (not in UniGene) with exon 2.23 PRSC_con, PC3, MB-MDA-231 324926 H56196 Hs.117798 ESTs 2.23 EB, EB, DU145 333632 CH22_FGENES.227_3 2.23 CALU6, CALU6, MB-MDA-453 328243 CH.06_hs gi|6056292 2.23 PC3, LnCap, LnCap 327037 CH.21_hs gi|6531965 2.23 LnCap, DU145, EB 307380 AI222985 EST singleton (not in UniGene) with exon 2.23 NCI-H345, PRSC_con, PRSC_log 334766 CH22_FGENES.428_15 2.23 PRSC_log, NCI-H345, RPWE-2 335236 CH22_FGENES.515_8 2.23 OVCA-R, MCF7, BT474 336615 CH22_FGENES.613_5 2.23 NCI-H69, PRSC_log, PRSC_con 307558 AI281998 EST singleton (not in UniGene) with exon 2.23 DU145, OVCA-R, CALU6 308029 AI457115 Hs.62954 ferritin; heavy polypeptide 1 2.23 EB, OVCA-R, MB-MDA-453 331508 N47559 Hs.46732 EST 2.23 MB-MDA-453, MCF7, BT474 320980 AJ237672 Hs.214142 5;10-methylenetetrahydrafolate reductase 2.23 OVCA-R, EB, EB 304241 AA010976 EST singleton (not in UniGene) with exon 2.23 BT474, MB-MDA-435s, MB-MDA-231 314682 AI190864 Hs.178226 ESTs; Weakly similar to !!!! ALU SUBFAMI 2.23 MB-MDA-231, MCF7, OVCA-R 308382 AI624301 EST singleton (not in UniGene) with exon 2.22 OVCA-R, BT474, CALU6 314476 AW207857 Hs.169604 ESTs 2.22 DU145, EB, A549 327864 CH.06_hs gi|5868130 2.22 NCI-H69, PRSC_log, PRSC_con 337279 CH22_FGENES.665-2 2.22 NCI-H345, NCI-H69, PRSC_con 302263 AA325517 EST 2.22 BT474, NCI-H520, DU145 322840 AA083710 EST cluster (not in UniGene) 2.22 HT29, MB-MDA-453, CALU6 307574 AI283549 EST singleton (not in UniGene) with exon 2.22 OVCA-R, CALU6, BT474 319027 AA716812 EST cluster (not in UniGene) 2.22 LnCap, NCI-H69, NCI-H69 305925 AA877883 EST singleton (not in UniGene) with exon 2.22 NCI-H345, NCI-H69, NCI-H69 329725 CH.14_p2 gi|6065785 2.22 NCI-H69, PRSC_con, NCI-H345 316194 AW298529 Hs.255774 ESTs 2.22 CALU6, EB, NCI-H520 301119 AF142579 EST 2.22 A549, OVCA-R, EB 333815 CH22_FGENES.282_4 2.22 MB-MDA-435s, EB, MB-MDA-453 334358 CH22_FGENES.378_1 2.22 NCI-H345, RPWE-2, PRSC_con 303763 AF043250 Hs.30928 DNA segment on chromosome 19 (unique) 11 2.21 Caco2, NCI-H23, NCI-H520 335593 CH22_FGENES.581_32 2.21 NCI-H345, PRSC_log, RPWE-2 334026 CH22_FGENES.318_3 2.21 NCI-H69, PRSC_con, NCI-H345 322224 AF086064 EST cluster (not in UniGene) 2.21 PRSC_con, PRSC_log, RPWE-2 309836 AW295497 Hs.157397 ESTs 2.21 NCI-H345, PRSC_con, RPWE-2 332669 M33374 Hs.661 NADH dehydrogenase (ubiquinone) 1 betas 2.21 NCI-H520, CALU6, OVCA-R 307629 AI300246 EST singleton (not in UniGene) with exon 2.21 MB-MDA-231, MB-MDA-453, HT29 300470 T87841 EST 2.21 PC3, EB, CALU6 330084 CH.19_p2 gi|6165044 2.21 NCI-H69, PRSC_con, BT474 338819 CH22_DJ246D7.GENSCAN.1-24 2.21 NCI-H69, RPWE-2, PRSC_log 337797 CH22_EM:AC005500.GENSCAN.3-4 2.21 LnCap, NCI-H69, NCI-H520 328025 CH.06_hs gi|5902482 2.2 RPWE-2, PRSC_con, PRSC_log 326240 CH.17_hs gi|5867260 2.2 EB, LnCap, MB-MDA-453 312865 AW005376 Hs.173280 ESTs 2.2 DU145, DU145, OVCA-R 338450 CH22_EM:AC005500.GENSCAN.359-36 2.2 MCF7, MB-MDA-453, MB-MDA-435s 302532 U60181 Hs.248115 growth hormone secretagogue receptor 2.2 PRSC_con, PRSC_log, PRSC_log 321132 AA081495 EST cluster (not in UniGene) 2.2 NCI-H23, NCI-H520, NCI-358 337787 CH22_EM:AC000097.GENSCAN.123-3 2.2 EB, PC3, LnCap 337032 CH22_FGENES.438-3 2.2 NCI-H69, NCI-H345, RPWE-2 300026 M11507 AFFX control: transferrin receptor 2.2 HT29, EB, MB-MDA-231 333139 CH22_FGENES.83_16 2.2 HT29, MB-MDA-453, Caco2 334298 CH22_FGENES.372_4 2.2 PRSC_con, PRSC_log, RPWE-2 335002 CH22_FGENES.470_7 2.2 PRSC_con, NCI-H345, NCI-H345 335000 CH22_FGENES.470_5 2.2 EB, PC3, A549 337298 CH22_FGENES.678-3 2.2 NCI-H69, A549, HT29 302481 AF104253 Hs.241381 cofactor required for Sp1 transcriptiona 2.2 EB, CALU6, LnCap 334819 CH22_FGENES.436_15 2.19 CALU6, BT474, Caco2 300426 AW452660 Hs.253296 ESTs 2.19 DU145, CALU6, HT29 302569 AC004472 multiple UniGene matches 2.19 RPWE-2, PRSC_log, PRSC_con 339401 CH22_BA232E17.GENSCAN.7-7 2.19 NCI-H345, NCI-H69, PRSC_log 328791 CH.07_hs gi|5868309 2.19 DU145, PC3, HT29 337333 CH22_FGENES.711-3 2.19 NCI-H69, NCI-H345, PRSC_log 339363 CH22_BA354I12.GENSCAN.33-6 2.19 NCI-H69, PRSC_log, PRSC_con 329429 CH.Y_hs gi|5868882 2.19 CALU6, HT29, OVCA-R 336927 CH22_FGENES.348-3 2.19 NCI-869, PRSC_log, NCI-358 336351 CH22_FGENES.816_3 2.19 DU145, EB, MB-MDA-231 313466 AA004731 Hs.148876 ESTs 2.19 CALU6, DU145, OVCA-R 307433 AI244895 EST singleton (not in UniGene) with exon 2.19 NCI-H23, NCI-H23, NCI-358 336590 CH22_FGENES.51_2 2.19 PRSC_con, NCI-H69, PRSC_log 310758 AI770001 Hs..209445 ESTs 2.18 EB, MB-MDA-231, BT474 327823 CH.05_hs gi|5867968 2.18 PRSC_con, NCI-H69, NCI-H345 313257 N92638 EST cluster (not in UniGene) 2.18 PRSC_log, RPWE-2, PRSC_con 335377 CH22_FGENES.543_17 2.18 PC3, MB-MDA-435s, CALU6 303958 AL042931 EST singleton (not in UniGene) with exon 2.18 NCI-H345, RPWE-2, PRSC_con 320153 AF064594 Hs.120360 phospholipase A2; group VI 2.18 LnCap, PC3, MB-MDA-435s 335201 CH22_FGENES.508_10 2.18 OVCA-R, DU145, HT29 338591 CH22.EMAC005500.GENSCAN.434-4 2.18 NCI-H69, NCI-H345, RPWE-2 331958 AA455960 Hs.99405 ESTs 2.18 MCF7, NCI-H23, NCI-H460 337218 CH22_FGENES.614-2 2.18 CALU6, A549, MCF7 309470 AW118833 EST singleton (not in UniGene) with exon 2.18 PC3, EB, MB-MDA-435s 331896 AA435495 Hs.97174 H sapiens mRNA; cDNA DKFZp566E164 (from 2.18 RPWE-2, NCI-H69, PRSC_log 330275 CH.05_p2 gi|6671904 2.18 NCI-H345, PRSC_log, PRSC_con 335817 CH22_FGENES.618_5 2.18 A549, Caco2, PC3 332896 CH22_FGENES.35_10 2.18 NCI-H345, RPWE-2, PRSC_log 303294 AA205300 EST 2.17 MB-MDA-435s, A549, MCF7 338703 CH22_EM:AC005500.GENSCAN.480-2 2.17 HT29, BT474, NCI-H69 300115 AI215044 Hs.208130 ESTs 2.17 PC3, OVCA-R, HT29 330979 H22466 Hs.31795 ESTs 2.17 MCF7, EB, MB-MDA-435s 317246 AW105092 Hs.155690 ESTs 2.17 MB-MDA-453, DU145, EB 329078 CH.X_hs gi|5868597 2.17 MB-MDA-453, MB-MDA-231, BT474 312554 AI222630 Hs.109390 ESTs 2.17 NCI-H520, OVCA-R, MCF7 323207 AI052795 Hs.192201 ESTs 2.17 NCI-H69, NCI-H345, PRSC_log 301894 AA484435 Hs.41997 alpha-1-B glycoprotein 2.17 PRSC_con, LnCap, PRSC_log 329097 CH.X_hs gi|5868624 2.16 MB-MDA-231, MCF7, NCI-358 328328 CH.07_hs gi|5868375 2.16 NCI-H345, PRSC_con, NCI-H69 302671 AA522440 Hs.135917 ESTs 2.16 BT474, DU145, A549 329201 CH.X_hs gi|5868718 2.16 OVCA-R, PC3, MB-MDA-435s 329902 CH.15_p2 gi|6634760 2.16 PRSC_con, NCI-H69, NCI-H345 334435 CH22_FGENES.385_10 2.16 PRSC_con, NCI-H345, RPWE-2 330742 AA400979 Hs.25691 calcitonin receptor-like receptor activi 2.16 MCF7, MB-MDA-453, PC3 328484 CH.07_hs gi|5868454 2.16 NCI-H69, PRSC_log, NCI-H345 334784 CH22_FGENES.432_9 2.16 PRSC_log, RPWE-2, PRSC_con 337771 CH22.EM:AC000097.GENSCAN.119-10 2.16 NCI-H69, PRSC_con, RPWE-2 300181 AI284955 Hs.157568 ESTs; Weakly similar to ataxin-2 [M.musc 2.16 DU145, EB, CALU6 300268 AI539446 Hs.245450 ESTs 2.16 PRSC_con, RPWE-2, PRSC_log 309575 AW168096 Hs.195188 glyceraldehyde-3-phosphate dehydrogenase 2.16 A549, NCI-H23, MB-MDA-453 336548 CH22_FGENES.841_5 2.16 NCI-H345, NCI-H69, MB-MDA-231 328506 CH.07_hs gi|5868471 2.16 EB, A549, CALU6 330189 CH.05_p2 gi|6165182 2.16 NCI-H460, MCF7, MB-MDA-453 305480 AA746500 Hs.25911 HLA-B associated transcript-2 2.16 EB, DU145, NCI-358 302270 R56151 EST 2.16 OVCA-R, MB-MDA-435s, PRSC_con 306669 AI004899 EST singleton (not in UniGene) with exon 2.16 PRSC_log, PRSC_con, NCI-H345 325887 CH.16_hs gi|5867087 2.16 EB, CALU6, NCI-358 327015 CH.21_hs gi|5867664 2.15 EB, PC3, HT29 338576 CH22_EM:AC005500.GENSCAN.429-1 2.15 NCI-H69, NCI-H345, PRSC_con 333592 CH22_FGENES.209_2 2.15 NCI-H69, OVCA-R, PRSC_con 317253 AW071241 Hs.199685 ESTs 2.15 MB-MDA-435s, NCI-H23, MB-MDA-453 302301 R67493 Hs.127150 ESTs; Weakly similar to ZINC FINGER PROT 2.15 PC3, MCF7, MB-MDA-435s 336858 CH22_FGENES.293-8 2.15 RPWE-2, PRSC_con, NCI-H69 308417 AI640693 Hs.2186 eukaryotic translation elongation factor 2.15 EB, OVCA-R, CALU6 338177 CH22_EM:AC005500.GENSCAN.219-5 2.15 NCI-H345, NCI-H23, NCI-H520 337592 CH22_C20H12.GENSCAN.6-7 2.15 PC3, A549, HT29 325945 CH.16_hs gi|5867138 2.15 MB-MDA-453, MB-MDA-435s, DU145 335262 CH22_FGENES.520_3 2.15 EB, PC3, A549 333665 CH22_FGENES.244_1 2.15 PRSC_con, RPWE-2, PRSC_log 333710 CH22_FGENES.250_25 2.14 PRSC_log, NCI-H69, PRSC_con 304927 AA604728 Hs.195188 glyceraldehyde-3-phosphate dehydrogenase 2.14 LnCap, PC3, MCF7 336999 CH22_FGENES.417-20 2.14 NCI-H69, NCI-H345, PRSC_con 313283 W32480 Hs.157099 ESTs 2.14 EB, MB-MDA-231, A549 306221 AA928686 EST singleton (not in UniGene) with exon 2.14 NCI-H460, PRSC_con, NCI-H23 333205 CH22_FGENES.102_5 2.14 NCI-H69, PRSC_con, PRSC_log 312932 AI804218 Hs.209614 ESTs 2.14 PRSC_con, NCI-H345, RPWE-2 328938 CH.08_hs gi|5868500 2.14 HT29, PC3, MB-MDA-453 326748 CH.20_hs gi|5867611 2.14 NCI-H345, NCI-H69, PRSC_con 337964 CH22_EM:AC005500.GENSCAN.100-9 2.14 RPWE-2, PRSC_con, PRSC_log 337984 CH22_EM:AC005500.GENSCAN.110-2 2.14 EB, DU145, NCI-H345 337704 CH22_EM.AC000097.GENSCAN.87-6 2.14 NCI-H69, NCI-H460, NCI-358 302162 AF119046 EST 2.14 MB-MDA-435s, PC3, EB 303192 AA081755 Hs.8059 ESTs; Highly similar to SYNAPTOTAGMIN IV 2.14 MB-MDA-435s, MB-MDA-435s, MB-MDA-453 306200 AA926816 EST singleton (not in UniGene) with exon 2.14 MB-MDA-453, CALU6, DU145 303996 AW515979 Hs.84298 CD74 antigen (invanant polypptd of majo 2.14 LnCap, MB-MDA-231, BT474 325409 CH.12_hs gi|5866921 2.14 PRSC_log, PRSC_con, RPWE-2 308558 AI700145 Hs.172182 poly(A)-binding protein; cytoplasmic 1 2.14 MCF7, ER, MB-MDA-435s 302185 AA243837 Hs.156915 ESTs 2.14 MB-MDA-453, MCF7, EB 303021 W39612 EST 2.14 PRSC_con, NCI-H69, RPWE-2 301005 AW451916 Hs.210848 ESTs 2.14 DU145, EB, HT29 336029 CH22_FGENES.672_4 2.14 NCI-H69, PRSC_con, RPWE-2 305443 AA736653 EST singleton (not in UniGene) with exon 2.14 NCI-358, NCI-H520, NCI-H23 335485 CH22_FGENES.570_17 2.13 NCI-H460, MB-MDA-435s, MCF7 304817 AA584712 EST singleton (not in UniGene) with exon 2.13 MCF7, MCF7, NCI-H520 309859 AW298760 EST singleton (not in UniGene) with exon 2.13 NCI-H69, PRSC_con, LnCap 326206 CH.17_hs gi|5867219 2.13 EB, MB-MDA-231, LnCap 303656 AA437189 Hs.122574 ESTs 2.13 LnCap, MB-MDA-435s, EB 334745 CH22_FGENES.426_3 2.13 OVCA-R, DU145, MB-MDA-453 318504 T26453 EST cluster (not in UniGene) 2.13 RPWE-2, LnCap, CALU6 306839 AI077385 EST singleton (not in UniGene) with exon 2.13 MCF7, MB-MDA-453, MB-MDA-435s 303843 W94322 Hs.58094 melanoma inhibitory activity 2.13 MB-MDA-435s, NCI-H345, RPWE-2 308444 AI659398 Hs.197097 EST 2.13 MB-MDA-453, MCF7, BT474 301322 AW448965 Hs.256305 ESTs 2.13 NCI-H345, LnCap, PC3 326997 CH.21_hs gi|5867660 2.13 HT29, A549, CALU6 326793 CH.20_hs gi|5867631 2.13 PRSC_log, PRSC_con, MB-MDA-453 320360 H12405 EST cluster (not in UniGene) 2.12 MB-MDA-231, BT474, HT29 316301 AW206279 Hs.192009 ESTs 2.12 DU145, DU145, EB 335371 CH22_FGENES.543_9 2.12 PC3, MB-MDA-435s, DU145 301178 AA828385 EST 2.12 EB, OVCA-R, LnCap 326136 CH.17_hs gi|5867202 2.12 RPWE-2, PRSC_log, PRSC_con 339213 CH22_FF113D11.GENSCAN.6.8 2.12 OVCA-R, PC3, MB-MDA-231 335980 CH22_FGENES.653_2 2.12 BT474, BT474, OVCA-R 314380 AA758797 Hs.192807 ESTs 2.11 PRSC_con, PRSC_log, RPWE-2 306779 AI041302 EST singleton (not in UniGene) with exon 2.11 NCI-H345, PRSC_con, PRSC_log 335774 CH22_FGENES.607_10 2.11 PC3, A549, MB-MDA-453 334914 CH22_FGENES.457_3 2.11 PRSC_con, NCI-H345, NCI-H69 304619 AA515554 Hs.119598 ribosomal protein L3 2.11 EB, MB-MDA-453, MB-MDA-435s 303358 AI199714 Hs.158149 ESTs 2.11 CALU6, OVCA-R, DU145 306558 AA994743 EST singleton (not in UniGene) with exon 2.11 HT29, MB-MDA-453, CALU6 337781 CH22_EM:AC000097.GENSCAN.121-3 2.11 PRSC_log, PRSC_con, RPWE-2 333140 CH22_FGENES.84_1 2.11 HT29, NCI-H69, OVCA-R 315081 AI247134 Hs.155281 ESTs 2.11 MB-MDA-453, MCF7, HT29 302965 AA446441 Hs.138842 ESTs 2.11 NCI-358, NCI-H23, CALU6 302138 N83965 EST 2.11 PRSC_log, PRSC_con, NCI-H345 320802 D83824 Hs.185055 BENE protein 2.11 A549, PC3, HT29 322152 AA565332 EST cluster (not in UniGene) 2.11 A549, CALU6, EB 326418 CH.19_hs gi|5867365 2.1 EB, OVCA-R, DU145 308709 AI783498 Hs.181165 eukaryotic translation elongation factor 2.1 MB-MDA-435s, MB-MDA-453, DU145 332737 C01852 Hs.84359 hypothetical protein 2.1 NCI-H23, A549, DU145 333283 CH22_FGENES.128_13 2.1 NCI-H345, RPWE-2, PRSC_con 328636 CH.07_hs gi|6004473 2.1 DU145, EB, MB-MDA-453 329187 CH.X_hs gi|5868713 2.1 NCI-358, NCI-H23, NCI-H460 305999 AA889603 EST singleton (not in UniGene) with exon 2.1 HT29, OVCA-R, PC3 333220 CH22_FGENES.104_12 2.1 PRSC_con, PRSC_log, RPWE-2 335092 CH22_FGENES.492_2 2.1 NCI-H69, PRSC_con, NCI-H345 304887 AA599355 EST singleton (not in UniGene) with exon 2.1 DU145, EB, MCF7 325359 CH.12_hs gi|5866920 2.1 MB-MDA-453, EB, MB-MDA-435s 330956 H08730 Hs.6933 ESTs 2.1 NCI-H520, PRSC_con, NCI-H345 323786 AW449315 Hs.165795 ESTs 2.1 OVCA-R, A549, LnCap 333619 CH22_FGENES.219_3 2.1 BT474, OVCA-R, HT29 324538 AW502979 EST cluster (not in UniGene) 2.09 CALU6, A549, DU145 303405 AA308601 EST 2.09 DU145, CALU6, NCI-H69 328570 CH.07_hs gi|5868231 2.09 LnCap, MB-MDA-231, DU145 308971 AI871218 Hs.224731 EST 2.09 NCI-H23, NCI-H460, NCI-358 330467 K02268 Hs.22584 prodynorphin 2.09 PC3, BT474, MB-MDA-453 334793 CH22_FGENES.433_5 2.09 EB, DU145, LnCap 300908 AA618335 Hs.146137 ESTs; Weakly similar to putative [C.eleg 2.09 NCI-H345, PRSC_log, PRSC_con 309656 AW197060 Hs.195188 glyceraldehyde-3-phosphate dehydrogenase 2.09 A549, NCI-H23, NCI-H460 320963 AB029041 Hs.209646 KIAA1118 protein 2.09 PRSC_con, PRSC_log, NCI-H345 310833 AW295351 Hs.169136 ESTs 2.09 PC3, LnCap, MB-MDA-453 335693 CH22_FGENES.596_8 2.09 NCI-H69, LnCap, PRSC_log 325966 CH.16_hs gi|5867147 2.09 MCF7, CALU6, MB-MDA-453 329319 CH.X_hs gi|6381976 2.09 NCI-H460, EB, DU145 338526 CH22_EM:AC005500.GENSCAN.396-14 2.09 NCI-H69, NCI-H345, PRSC_log 336751 CH22_FGENES.128-5 2.09 NCI-H69, NCI-H345, PRSC_log 325510 CH.12_hs gi|5866974 2.09 HT29, OVCA-R, CALU6 323553 AA292626 Hs.122854 ESTs 2.08 NCI-H345, RPWE-2, NCI-358 326343 CH.17_hs gi|8525295 2.08 EB, LnCap, DU145 335470 CH22_FGENES.568_3 2.08 NCI-H69, PRSC_con, PRSC_log 320122 T93681 Hs.187515 ESTs 2.08 MCF7, MB-MDA-453, BT474 335320 CH22_FGENES.534_7 2.08 BT474, MB-MDA-231, HT29 307120 AI184343 EST singleton (not in UniGene) with exon 2.08 HT29, MCF7, PC3 338080 CH22_EM:AC005500.GENSCAN.172-11 2.08 LnCap, PC3, HT29 313113 AI056258 Hs.122523 ESTs 2.08 MCF7, DU145, MB-MDA-453 337685 CH22_EM:AC000097.GENSCAN.77-1 2.08 NCI-H69, NCI-H345, PRSC_log 327461 CH.02_hs gi|6004455 2.08 NCI-H23, BT474, NCI-358 335895 CH22_FGENES.635_3 2.08 HT29, MB-MDA-231, NCI-H520 303933 AW471472 EST singleton (not in UniGene) with exon 2.08 MS-MDA-231, BT474, NCI-H345 314803 AI935159 Hs.166841 ESTs; Weakly similar to MYOSIN LIGHT CHA 2.08 PC3, A549, BT474 NON-MUSCLE ISOZYMES [H.sapiens] 302722 U53530 EST 2.08 DU145, MB-MDA-435s, OVCA-R 307703 AI318588 EST singleton (not in UniGene) with exon 2.08 HT29, MB-MDA-435s, CALU6 310558 AI334965 Hs.176976 ESTs 2.08 A549, LnCap, PC3 315276 AA860090 EST cluster (not in UniGene) 2.08 PC3, MCF7, OVCA-R 306443 AA976950 EST singleton (not in UniGene) with exon 2.07 OVCA-R, PC3, EB 307961 AI421059 EST singleton (not in UniGene) with exon 2.07 HT29, OVCA-R, CALU6 329735 CH.14_p2 gi|6065780 2.07 EB, HT29, OVCA-R 335193 CH22_FGENES.507_8 2.07 EB, A549, A549 320347 R34423 Hs.221535 ESTs 2.07 CALU6, A549, EB 316153 AA724474 Hs.147208 ESTs 2.07 MS-MDA-453, PC3, HT29 300921 AW293224 Hs.232165 ESTs 2.07 HT29, CALU6, CALU6 319264 T65096 EST cluster (not in UniGene) 2.07 MS-MDA-453, MCF7, CALU6 330204 CH.05_p2 gi|6013606 2.07 OVCA-R, DU145, EB 317070 AI142037 Hs.125379 ESTs 2.07 PRSC_con, NCI-H345, OVCA-R 337645 CH22.EM:AC000097.GENSCAN.10-8 2.07 NCI-H345, PRSC_log, NCI-H69 312501 AW450490 Hs.132886 ESTs 2.07 NCI-H520, CALU6, MCF7 335587 CH22_FGENES.581_26 2.07 NCI-H69, NCI-H345, PRSC_log 311482 AI917706 Hs.129997 ESTs 2.07 NCI-H520, MCF7, MS-MDA-435s 302488 AF161441 EST 2.07 EB, DU145, CALU6 304692 AA554202 Hs.76067 heat shock 27 kD protein 1 2.07 MCF7, MB-MDA-453, PC3 325369 CH.12_hs gi|5866920 2.07 DU145, DU145, MS-MDA-453 306284 AA936835 EST singleton (not in UniGene) with exon 2.07 BT474, MB-MDA-231, HT29 337402 CH22_FGENES.752-1 2.07 A549, BT474, DU145 327418 CH.02_hs gi|5867750 2.07 MCF7, MB-MDA-453, MB-MDA-435s 317977 AI004775 Hs.205091 ESTs; Weakly similar to WW domain bindin 2.07 BT474, MB-MDA-453, PC3 331870 AA428560 Hs.161845 EST 2.07 MB-MDA-231, MB-MDA-435s, BT474 300750 AA514805 Hs.105464 ESTs 2.07 HT29, BT474, BT474 336657 CH22_FGENES.35-14 2.07 MB-MDA-453, MCF7, NCI-H460 336035 CH22_FGENES.678_6 2.07 NCI-H69, PRSC_con, RPWE-2 325320 CH.11_hs gi|5866870 2.06 NCI-H69, PRSC_log, PRSC_con 306053 AA905312 EST singleton (not in UniGene) with exon 2.06 HT29, OVCA-R, MB-MDA-231 333175 CH22_FGENES.95_2 2.06 LnCap, HT29, DU145 304491 AA437096 Hs.115502 EST 2.06 MB-MDA-435s, CALU6, CALU6 310632 AI697536 Hs.176991 ESTs 2.06 NCI-H69, PRSC_log, NCI-H345 338521 CH22_EMAC005500.GENSCAN.395-35 2.06 NCI-H345, PRSC_log, PRSC_log 334900 CH22_FGENES.452_14 2.06 A549, CALU6, NCI-H69 337451 CH22_FGENES.774-2 2.06 PRSC_con, PRSC_log, RPWE-2 306792 AI815153 Hs.195188 glyceraldehyde-3-phosphate dehydrogenase 2.06 DU145, BT474, MB-MDA-453 336854 CH22_FGENES.280-1 2.06 LnCap, EB, MB-MDA-435s 304485 AA434076 EST singleton (not in UniGene) with exon 2.06 MB-MDA-231, BT474, CALU6 326458 CH.19_hs gi|5867400 2.06 EB, DU145, LnCap 303506 AA340605 Hs.105887 ESTs 2.06 LnCap, MCF7, CALU6 333628 CH22_FGENES.226_2 2.06 NCI-H520, NCI-358, NCI-358 300763 AA190753 EST 2.06 NCI-H69, NCI-H345, PRSC_con 334836 CH22_FGENES.439_6 2.06 NCI-H345, PRSC_con, RPWE-2 335217 CH22_FGENES.512_3 2.06 PRSC_log, PRSC_con, NCI-H69 338970 CH22_DJ32I10.GENSCAN.26-3 2.06 A549, MB-MDA-453, LnCap 334842 CH22_FGENES.439_21 2.06 DU145, HT29, CALU6 309309 AW006428 Hs.232857 EST 2.06 EB, DU145, OVCA-R 332949 CH22_FGENES.47_12 2.06 EB, DU145, OVCA-R 310530 AW369663 Hs.150150 ESTs 2.06 PRSC_con, PRSC_log, RPWE-2 329401 CH.X_hs gi|6682544 2.06 NCI-H69, PRSC_con, RPWE-2 316893 AA837332 EST duster (not in UniGene) 2.06 OVCA-R, MCF7, MR-MDA-453 325022 W95840 Hs.59745 NADH dehydrogenase (ubiquinone) flavopro 2.06 Caco2, NCI-358, OVCA-R 329839 CH.14_p2 gi|6672062 2.05 MB-MDA-231, RPWE-2, CALU6 306668 AI004890 EST singleton (not in UniGene) with exon 2.05 DU145, MB-MDA-453, MCF7 315604 AW137442 Hs.136965 ESTs 2.05 LnCap, EB, PC3 318551 AI909951 Hs.239307 tyrosyl-tRNA synthetase 2.05 NCI-H345, PRSC_con, RPWE-2 339344 CH22_BA354I12.GENSCAN.28-1 2.05 BT474, MR-MDA-231, A549 310621 AI632098 Hs.198099 ESTs 2.05 NCI-H69, RPWE-2, MCF7 327051 CH.21_hs gi|6531965 2.05 PRSC_con, NCI-H345, PRSC_log 336827 CH22_FGENES.236-2 2.05 NCI-H345, A549, MB-MDA-231 311846 AI078033 Hs.177170 ESTs; Moderately similar to !!!! ALU SUB 2.05 OVCA-R, DU145, CALU6 335036 CH22_FGENES.475_14 2.05 NCI-H69, PRSC_con, NCI-H345 313100 N52880 Hs.122817 ESTs 2.05 RPWE-2, NCI-H345, PRSC_log 301927 AF014459 Hs.113250 retinoschisis (X-linked; juvenile) 1 2.05 MB-MDA-231, NCI-H345, PRSC_con 326070 CH.17_hs gi|5867175 2.05 MB-MDA-435s, MB-MDA-231, BT474 338514 CH22_EM:AC005500.GENSCAN.392-4 2.05 PRSC_con, PRSC_log, RPWE-2 328098 CH.06_hs gi|5868020 2.05 DU145, CALU6, EB 301102 AA679361 Hs.249487 ESTs 2.05 NCI-H460, PRSC_con, NCI-H23 306193 AA923457 EST singleton (not in UniGene) with exon 2.05 NCI-H345, PRSC_con, RPWE-2 317027 AA883808 Hs.174148 ESTs 2.05 EB, DU145, CALU6 336102 CH22_FGENES.693_2 2.04 LnCap, NCI-H69, PRSC_log 301372 AI239895 Hs.130555 ESTs 2.04 PRSC_con, RPWE-2, PRSC_log 333252 CH22_FGENES.116_4 2.04 NCI-358, A549, HT29 322516 AW372340 Hs.159717 ESTs 2.04 HT29, MB-MDA-231, BT474 324146 AA393624 EST cluster (not in UniGene) 2.04 RPWE-2, PRSC_con, MB-MDA-231 338770 CH22_EM:AC005500.GENSCAN.520-1 2.04 PRSC_con, NCI-H69, NCI-H460 314795 AI798611 Hs.157277 ESTs 2.04 EB, PC3, LnCap 333004 CH22_FGENES.60_1 2.04 A549, NCI-358, DU145 302405 AW245825 Hs.211914 NADH dehydrogenase (ubiquinone) Fe-S pro 2.04 NCI-H520, CALU6, Caco2 323587 AI905527 Hs.141901 ESTs; Moderately similar to !!!! ALU SUB 2.04 EB, A549, HT29 300898 AI276278 Hs.157176 ESTs 2.04 PC3, MR-MDA-453, BT474 301506 AI149878 Hs.143519 ESTs; Weakly similar to testicular tekti 2.04 NCI-H69, RPWE-2, NCI-H345 325851 CH.16_hs gi|5867067 2.04 MB-MDA-231, HT29, EB 323945 AI125604 Hs.155117 ESTs 2.04 MCF7, DU145, DU145 303265 AW160951 EST 2.04 LnCap, OVCA-R, DU145 334135 CH22_FGENES.336_2 2.04 PC3, A549, MB-MDA-435s 329793 CH.14_p2 gi|8522661 2.04 DU145, CALU6, HT29 332595 AA256431 Hs.3244 G protein pathway suppressor 2 2.04 A549, CALU6, NCI-H23 316059 AW166388 Hs.250181 ESTs 2.04 MCF7, HT29, A549 324104 AW248071 Hs.133122 ESTs 2.04 Caco2, A549, MCF7 306801 AI052653 EST singleton (not in UniGene) with exon 2.03 EB, LnCap, PC3 338096 CH22.EM:AC005500.GENSCAN.181-14 2.03 DU145, HT29, CALU6 327544 CH.03_hs gi|5867797 2.03 PRSC_con, NCI-H69, NCI-H345 318813 F13195 EST cluster (not in UniGene) 2.03 PRSC_con, RPWE-2, PRSC_log 325289 CH.11_hs gi|5866903 2.03 EB, OVCA-R, A549 311099 T56361 Hs.182167 hemoglobin: gamma A 2.03 HT29, RT474, EB 316079 AA922213 Hs.121735 ESTs 2.03 LnCap, OVCA-R, EB 309533 AW151131 EST singleton (not in UniGene) with exon 2.03 MB-MDA-231, BT474, LnCap 338579 CH22.EM:AC005500.GENSCAN.431-3 2.03 NCI-H69, NCI-H345, RPWE-2 326549 CH.19_hs gi|5867307 2.03 NCI-H69, Caco2, NCI-H345 320012 AI628384 Hs.193745 ESTs 2.03 BT474, MB-MDA-453, MCF7 334111 CH22_FGENES.330_10 2.03 NCI-H69, MB-MDA-231, BT474 327123 CH.21_hs gi|6531971 2.03 NCI-H345, NCI-H69, RPWE-2 324568 AW502311 EST cluster (not in UniGene) 2.03 NCI-H345, NCI-H520, NCI-H460 306012 AA896989 EST singleton (not in UniGene) with exon 2.03 NCI-H69, PRSC_log, PRSC_con 303106 AA012877 EST 2.03 RPWE-2, OVCA-R, EB 302194 U52219 Hs.158329 G protein-coupled receptor 50 2.03 NCI-H520, NCI-H23, PC3 326646 CH.20_hs gi|5867562 2.03 NCI-H460, OVCA-R, HT29 304060 T61464 EST singleton (not in UniGene) with exon 2.03 NCI-H345, PRSC_con, PRSC_log 304667 AA535602 EST singleton (not in UniGene) with exon 2.03 A549, DU145, EB 330514 M83652 Hs.53155 properdin P factor, complement 2.02 NCI-H23, NCI-H460, NCI-358 310324 AI473273 Hs.159674 ESTs; Weakly similar to GLUTAMATE [H.sap 2.02 NCI-H345, MB-MDA-231, BT474 330327 CH.08_p2 gi|5919194 2.02 NCI-H345, NCI-H69, PRSC_log 308447 AI659985 EST singleton (not in UniGene) with exon 2.02 NCI-H345, RPWE-2, PRSC_log 307778 AI344972 Hs.231496 EST 2.02 NCI-H69, CALU6, OVCA-R 319459 T87351 Hs.194121 ESTs 2.02 NCI-H460, NCI-358, NCI-H520 300935 AA513644 Hs.222815 ESTs; Weakly similar to Wiskott-Aldrich 2.02 DU145, EB, OVCA-R 314318 AL037405 Hs.176141 ESTs 2.02 PRSC_con, LnCap, PRSC_log 334779 CH22_FGENES.432_1 2.02 EB, HT29, DU145 336994 CH22_FGENES.410-2 2.02 NCI-H345, PRSC_con, NCI-H69 334076 CH22_FGENES.327_31 2.02 OVCA-R, CALU6, EB 318116 AW452865 Hs.132339 ESTs 2.02 MB-MDA-231, NCI-H69, NCI-H345 326783 CH.20_hs gi|6525298 2.02 NCI-H69, PRSC_con, RPWE-2 336142 CH22_FGENEB.705_4 2.02 NCI-H69, PRSC_log, PRSC_con 320913 AA663733 EST cluster (not in UniGene) 2.02 DU145, EB, CALU6 301644 AW239364 EST 2.02 PRSC_con, RPWE-2, PRSC_log 300944 AW081072 Hs.164624 ESTs; Weakly similar to Slit-3 protein [ 2.01 RPWE-2, NCI-H69, NCI-H23 310080 AW137088 Hs.144857 ESTs 2.01 PRSC_con, NCI-H345, PRSC_log 311246 AI863918 Hs.195078 ESTs 2.01 NCI-H345, NCI-H69, RPWE-2 319207 R87679 EST cluster (not in UniGene) 2.01 HT29, A549, NCI-H460 334760 CH22_FGENES.428_9 2.01 NCI-358, NCI-H69, PRSC_log 338368 CH22_EM:AC005500.GENSCAN.325-2 2.01 NCI-H23, NCI-H520, NCI-H460 317300 AI417007 Hs.166338 ESTs 2.01 NCI-H460, DU145, NCI-H23 323699 AW178750 EST cluster (not in UniGene) 2.01 MCF7, MB-MDA-453, OVCA-R 301366 AA907713 Hs.221667 ESTs 2.01 PRSC_con, NCI-H345, RPWE-2 333306 CH22_FGENES.137_3 2.01 NCI-H69, NCI-H345, PRSC_con 328031 CH.06_hs gi|5902482 2.01 MB-MDA-231, NCI-H345, PRSC_con 301806 AA326007 Hs.12056 asialoglycoprotein receptor 1 2.01 MB-MDA-453, DU145, EB 300993 AA584930 Hs.191777 ESTs; Weakly similar to XAP-5-like prote 2.01 HT29, NCI-H23, NCI-358 320042 T84520 EST cluster (not in UniGene) 2.01 PRSC_con, NCI-H345, NCI-H69 331082 R17059 Hs.22100 ESTs 2.01 EB, DU145, MB-MDA-435s 308851 AI829820 EST singleton (not in UniGene) with exon 2.01 DU145, EB, PC3 301163 AA732066 EST 2.01 OVCA-R, PC3, MB-MDA-435s 304734 AA576428 EST singleton (not in UniGene) with exon 2.01 LnCap, MB-MDA-453, DU145 334855 CH22_FGENES.442_6 2.01 NCI-H345, RPWE-2, PRSC_log 337121 CH22_FGENES.519-1 2.01 NCI-H69, NCI-H345, PRSC_con 331838 AA412498 Hs.104778 ESTs 2.01 BT474, BT474, MCF7 339181 CH22_DA59H18.GENSCAN.72-6 2.01 NCI-H345, PRSC_con, NCI-H69 327564 CH.03_hs gi|5867811 2.01 BT474, HT29, DU145 304108 R63932 Hs.28467 EST 2 BT474, OVCA-R, MCF7 315036 AA534953 Hs.163297 ESTs 2 MB-MDA-435s, MB-MDA-453, LnCap 312777 W92809 Hs.138557 ESTs 2 PRSC_con, NCI-H345, MB-MDA-231 305888 AA868536 Hs.126145 EST 2 HT29, HT29, BT474 323185 R52177 EST cluster (not in UniGene) 2 EB, A549, BT474 308681 AI761307 EST singleton (not in UniGene) with exon 2 RPWE-2, PRSC_con, NCI-H345 325755 CH.14_hs gi|6682474 2 NCI-H345, PRSC_con, PRSC_log 324376 AW499705 EST cluster (not in UniGene) 2 DU145, BT474, PC3 331890 AA432166 Hs.3577 succinate dehydrogenase complex; subunit 2 CALU6, MB-MDA-453, A549

[0330] TABLE 4 Pkey: Unique Eos probeset identifier number ExAccn: Exemplar Accession number, Genbank accession number UnigeneID: Unigene number Unigene Title: Unigene gene title Ratio Pkey Exr_Accn UniG_ID Complete_Title Met/BS Top 3 expressing cell lines 313166 AI801098 Hs.151500 ESTs 12.23 Caco2, EB, OVCA-R 334593 CH22_FGENES.408_3 8.06 NCI-H169, OVCA-R, OVCA-R 331084 R20655 Hs.81281 Human clone 23732 mRNA; partial cds 7.89 LnCap, OVCA-R, EB 324598 AA502659 Hs.163986 ESTs 7.77 OVCA-R, EB, CALU6 314071 AA192455 Hs.188690 ESTs 7.76 CALU6, EB, DU145 315178 AW362945 Hs.162459 ESTs 6.81 OVCA-R, EB, CALU6 325519 CH.12_hs gi|6017036 6.34 NCI-H69, NCI-H345, PRSC_con 331433 H68097 Hs.161023 EST 6.16 OVCA-R, A549, EB 315021 AA533447 EST cluster (not in UniGene) 6.15 PC3, EB, CALU6 337695 CH22_EM:AC000097.GENSCAN.84-1 5.84 NCI-H69, NCI-H345, DU145 324048 AA378739 EST cluster (not in UniGene) 5.77 OVCA-R, DU145, EB 300781 AA731209 EST cluster (not in UniGene) with exon h 5.72 MB-MDA-453, MCF7, MB-MDA-435s 320701 AI093177 Hs.134923 ESTs 5.68 A549, NCI-H345, NCI-H69 332471 AA416967 Hs.120980 nuclear receptor co-repressor 2 5.68 LnCap, A549, OVCA-R 331858 AA421163 Hs.163848 ESTs 5.66 OVCA-R, DU145, Caco2 330987 H40988 Hs.131965 ESTs 5.35 NCI-H345, OVCA-R, LnCap 322309 AF086372 EST cluster (not in UniGene) 5.31 OVCA-R, DU145, PC3 324733 AA582082 Hs.199410 ESTs 5.17 PRSC_con, PRSC_log, NCI-H345 313577 AA565051 Hs.155029 ESTs 5.16 OVCA-R, PC3, EB 310966 AW271974 Hs.210295 ESTs 5.15 NCI-H69, PRSC_log, PRSC_con 311332 AW292247 Hs.255052 ESTs 5.05 Caco2, OVCA-R, EB 314522 AI732331 Hs.187750 ESTs; Moderately similar to !!!! ALU CLA 5.04 EB, DU145, HT29 330886 AA135606 Hs.189384 ESTs; Weakly similar to !!!! ALU SUBFAMI 4.93 OVCA-R, DU145, Caco2 313597 AW162263 Hs.249990 ESTs 4.84 NCI-H460, NCI-H345, NCI-H23 314439 AI539443 Hs.137447 ESTs 4.84 DU145, Caco2, MB-MDA-231 320807 AA086110 Hs.188536 H sapiens clone 24838 mRNA seq 4.83 PC3, OVCA-R, DU145 311804 AA135159 Hs.203349 ESTs 4.82 OVCA-R, PC3, Caco2 321354 AA078493 EST cluster (not in UniGene) 4.81 DU145, EB, OVCA-R 325169 H01560 Hs.163818 ESTs; Weakly similar to !!!! ALU SUBFAMI 4.8 NCI-H345, DU145, LnCap 312828 AI865455 Hs.211818 ESTs; Moderately similar to !!!! ALU SUB 4.78 DU145, DU145, DU145 321226 AA311443 Hs.251416 H sapiens mRNA; cDNA DKFZp586E2317 (from 4.75 DU145, OVCA-R, MB-MDA-453 327772 CH.05_hs gi|5867964 4.74 HT29, MB-MDA-231, NCI-H345 315642 AA742222 Hs.120634 ESTs 4.7 DU145, EB, MB-MDA-453 311905 AA555215 Hs.151913 ESTs 4.7 DU145, Caco2, PRSC_con 312754 R99834 Hs.250383 ESTs 4.59 OVCA-R, PC3, EB 336637 CH22_FGENES.13-7 4.58 NCI-H69, PRSC_log, NCI-H345 331644 T99544 Hs.173734 ESTs; Weakly similar to !!!! ALU CLASS B 4.55 OVCA-R, NCI-H345, Caco2 336984 CH22_FGENES.401-2 4.55 Caco2, Caco2, EB 316261 AW134485 Hs.144967 ESTs 4.53 NCI-H460, NCI-H345, Caco2 300417 AW139492 Hs.245887 ESTs 4.52 DU145, CALU6, EB 300610 N72596 Hs.99120 DEAD/H (Asp-Glu-Ala-Asp/His) box polypep 4.52 OVCA-R, PC3, EB 324718 AI557019 Hs.116467 ESTs 4.5 LnCap, PC3, PRSC_con 332170 F04112 Hs.177178 ESTs 4.47 Caco2, DU145, DU145 324042 AA377589 EST cluster (not in UniGene) 4.45 NCI-H345, PRSC_con, PRSC_log 331148 R73816 Hs.17385 ESTs 4.44 CALU6, OVCA-R, EB 328981 CH.09_hs gi|5868527 4.43 HT29, BT474, NCI-H69 321920 N63915 EST cluster (not in UniGene) 4.34 Caco2, A549, A549 320832 AA214584 EST cluster (not in UniGene) 4.34 NCI-H23, CALU6, OVCA-R 321971 AI680459 Hs.201441 ESTs 4.33 DU145, HT29, CALU6 308572 AI707882 EST singleton (not in UniGene) with exon 4.33 MCF7, NCI-H345, OVCA-R 302459 AF169255 EST cluster (not in UniGene) with exon h 4.28 MB-MDA-231, OVCA-R, LnCap 321847 T08401 EST cluster (not in UniGene) 4.25 MB-MDA-453, MB-MDA-435s, MBS-MDA-231 337884 CH22_EM:AC005500.GENSCAN.54-2 4.23 HT29, NCI-H23, MB-MDA-435s 307494 AI269188 Hs.175656 EST 4.23 NCI-H23, NCI-H520, NCI-358 314915 AA573072 Hs.187748 ESTs; Weakly similar to !!!! ALU SUSFAMI 4.21 PC3, OVCA-R, Caco2 336638 CH22_FGENES.14-2 4.21 NCI-H69, NCI-H345, PRSC_log 319379 T91443 Hs.193963 ESTs 4.2 PC3, OVCA-R, LnCap 312332 R33041 Hs.106200 ESTs 4.19 NCI-H69, OVCA-R, NCI-H460 331445 H89093 Hs.41215 ESTs 4.19 EB, HT29, DU145 315841 AW138397 Hs.247572 ESTs 4.19 Caco2, MB-MDA-453, LnCap 315712 AI950133 Hs.120882 ESTs; Moderately similar to !!!! ALU SUB 4.18 LnCap, NCI-H345, OVCA-R 319559 AA773876 Hs.251597 ESTs 4.15 NCI-H345, Caco2, DU145 300791 AL138455 Hs.256135 ESTs; Moderately similar to !!!! ALU SUB 4.13 NCI-358, RPWE-2, NCI-H460 312129 AW300867 EST cluster (not in UniGene) 4.12 OVCA-R, MCF7, A549 321166 AA411263 Hs.128783 ESTs 4.11 QVCA-R, Caco2, PRSC_con 313220 AI971981 Hs.118241 ESTs 4.1 OVCA-R, DU145, Caco2 314022 AW452420 Hs.248678 ESTs 4.1 OVCA-R, EB, PC3 321359 AW474412 EST cluster (not in UniGene) 4.1 DU145, OVCA-R, PC3 328841 CH.07_hs gi|6381920 4.09 NCI-H69, PRSC_log, NCI-H345 337898 CH22_EM:AC005500.GENSCAN.56-5 4.09 NCI-H345, NCI-H69, OVCA-R 333245 CH22_FGENES.115_2 4.09 PRSC_log, PRSC_con, NCI-H345 311958 AI247472 Hs.132965 ESTs 4.06 EB, DU145, CALU6 314775 AI149880 Hs.188809 ESTs 4.06 OVCA-R, PC3, EB 317901 AW150944 Hs.250541 ESTs 4.06 BT474, MB-MDA-453, MB-MDA-435s 309985 AW452919 EST singleton (not in UniGene) with exon 4.05 MB-MDA-453, NCI-H23, NCI-H520 311004 AA632846 EST cluster (not in UniGene) 4.05 MB-MDA-453, OVCA-R, EB 323497 AI523613 Hs.221544 ESTs 4.04 LnCap, OVCA-R, EB 332347 W60326 Hs.221716 ESTs 4.04 EB, CALU6, PC3 331388 AA456852 Hs.43543 suppressor of whhe apricot homolog 2 4.01 A549, EB, Caco2 313197 AI738851 Hs.222487 ESTs 3.96 OVCA-R, EB, PC3 315710 AA931550 Hs.192785 ESTs 3.95 EB, MB-MDA-231, OVCA-R 316897 AA838114 EST cluster (not in UniGene) 3.94 OVCA-R, A549, MB-MDA-453 322564 W86440 Hs.118344 ESTs 3.94 NCI-H460, Caco2, EB 304605 AA513225 EST singleton (not in UniGene) with exon 3.9 NCI-H345, RPWE-2, BT474 325726 CH.14_hs gi|6552447 3.9 OVCA-R, LnCap, LnCap 320190 R32047 Hs.141012 ESTs; Weakly similar to !!!! ALU SUBFAMI 3.89 DU145, NCI-H23, PRSC_log 331566 N63062 Hs.48703 EST 3.87 NCI-H23, NCI-H460, NCI-358 319403 T98413 EST cluster (not in UniGene) 3.86 NCI-H345, PRSC_log, LnCap 324643 AI436356 Hs.130729 ESTs 3.84 OVCA-R, DU145, NCI-H345 315298 AI969314 Hs.211377 ESTs 3.82 NCI-H345, PRSC_con, PRSC_log 321632 AA419617 EST cluster (not in UniGene) 3.81 EB, OVCA-R, A549 313219 N74924 Hs.182099 ESTs 3.8 EB, Caco2, OVCA-R 330833 AA046804 ESTs; Weakly similar to !!!! ALU SUBFAMI 3.8 LnCap, DU145, PC3 327289 CH.01_hs gi|5867481 3.79 EB, HT29, DU145 314429 AW300749 EST cluster (not in UniGene) 3.79 OVCA-R, PC3, PRSC_con 314475 AI911160 Hs.127505 ESTs 3.79 DU145, CALU6, NCI-H69 317130 AW293995 Hs.192277 ESTs 3.78 EB, PC3, Caco2 336635 CH22_FGENES.13-5 3.77 NCI-H69, NCI-H345, PRSC_log 333323 CH22_FGENES.138_16 3.76 NCI-H460, NCI-H23, PRSC_con 332135 AA620331 Hs.245351 EST 3.75 NCI-H345, A549, Caco2 316979 AA861087 EST cluster (not in UniGene) 3.75 NCI-H345, NCI-H69, RPWE-2 316435 AI671871 Hs.192618 ESTs; Weakly similar to !!!! ALU CLASS C 3.74 MB-MDA-435s, MCF7, MB-MDA-453 316422 AW135357 Hs.192374 ESTs 3.73 OVCA-R, A549, EB 336616 CH22_FGENES.613_5 3.72 NCI-H69, NCI-H345, RPWE-2 320258 W93241 EST cluster (not in UniGene) 3.71 MB-MDA-231, NCI-H69, EB 300463 N52510 Hs.186470 ESTs 3.69 OVCA-R, A549, DU145 306881 AI088695 EST singleton (not in UniGene) with exon 3.68 CALU6, HT29, EB 337304 CH22_FGENES.681-6 3.67 MCF7, MB-MDA-453, LnCap 323693 AW297758 Hs.249721 ESTs 3.67 OVCA-R, MB-MDA-453, DU145 331073 R07998 Hs.18628 ESTs; Weakly similar to !!!! ALU SUBFAMI 3.67 RPWE-2, NCI-H345, OVCA-R 318162 AW296277 Hs.132171 ESTs 3.67 MB-MDA-231, DU145, CALU6 318042 AW294522 Hs.149991 ESTs 3.66 ES, HT29, CALU6 308069 AI470895 EST singleton (not in UniGene) with exon 3.64 Caco2, Caco2, NCI-H23 327614 CH.04_hs gi|6525283 3.62 NCI-H460, NCI-H345, NCI-H69 337514 CH22_FGENES.809.7 3.62 NCI-358, NCI-H23, NCI-H460 332093 AA608794 Hs.112592 ESTs 3.6 EB, OVCA-R, DU145 327793 CH.05_hs gi|5867979 3.59 LnCap, OVCA-R, EB 331053 N70242 Hs.183146 ESTs 3.59 OVCA-R, EB, Caco2 303769 AA134888 Hs.173415 ESTs 3.58 HT29, CALU6, CALU6 319872 R97130 Hs.189699 ESTs 3.58 PRSC_con, LnCap, RPWE-2 317902 AI828602 Hs.211265 ESTs 3.57 CALU6, NCI-H345, OVCA-R 324090 AI656531 Hs.116070 ESTs 3.57 PRSC_con, NCI-H345, PRSC_log 300120 AW204314 Hs.170784 ESTs 3.57 NCI-H69, NCI-H345, PRSC_con 307752 AI339447 EST singleton (not in UniGene) with exon 3.56 NCI-358, HT29, MB-MDA-231 322438 W44531 Hs.167851 ESTs 3.55 NCI-H345, NCI-H69, Caco2 311275 AI659166 Hs.207144 ESTs 3.55 MB-MDA-231, PRSC_con, LnCap 338830 CH22_DJ246D7.GENSCAN.6-7 3.54 LnCap, PC3, OVCA-R 315647 AA648983 Hs.212911 ESTs 3.53 OVCA-R, MB-MDA-453, CALU6 331469 N22273 Hs.39140 ESTs 3.52 EB, A549, CALU6 313445 AI123657 Hs.127264 ESTs 3.51 EB, OVCA-R, A549 330139 CH.21_432 gi|4210430 3.5 EB, CALU6, DU145 304450 AA404521 Hs.10326 coatomer protein complex: subunit epsilo 3.49 NCI-H345, NCI-H69, NCI-H460 325763 CH.14_hs gi|6682475 3.49 PC3, BT474, OVCA-R 312803 AA677934 Hs.117864 ESTs 3.47 OVCA-R, Caco2, MB-MDA-453 303654 AA436942 Hs.168308 ESTs 3.46 DU145, NCI-H460, NCI-H69 317924 AI222324 Hs.166306 ESTs; Weakly similar to zinc finger prot 3.46 PRSC_con, PRSC_log, NCI-H69 312354 AA036955 Hs.167040 ESTs 3.44 Caco2, MB-MDA-435s, NCI-H460 337517 CH22_FGENES.814-6 3.43 NCI-H69, HT29, PC3 324865 AA702138 Hs.114103 ESTs 3.42 NCI-H23, NCI-H460, NCI-H520 323755 AW300094 EST cluster (not in UniGene) 3.42 PRSC_con, RPWE-2, NCI-H345 314452 AL042699 Hs.209222 ESTs 3.42 NCI-H345, PRSC_con, PRSC_log 337911 CH22_EM:AC0055500.GENSCAN.59-6 3.42 OVCA-R, PC3, HT29 318086 AI025499 Hs.132238 ESTs 3.41 CALU6, LnCap, OVCA-R 311859 AA704705 Hs.181044 ESTs; Weakly similar to Chain A: Human O 3.41 LnCap, MB-MDA-435s, A549 Complexed With L-Canaline [H. sapiens] 314409 H15560 Hs.131833 ESTs 3.41 NCI-H69, LnCap, LnCap 323333 AA228883 EST cluster (not in UniGene) 3.41 Caco2, OVCA-R, NCI-H69 325690 CH.14_hs gi|5867021 3.4 HT29, CALU6, DU145 314539 AA398216 Hs.190092 ESTs 3.4 MB-MDA-231, BT474, EB 310567 AI691065 Hs.155780 ESTs 3.4 PRSC_con, NCI-H345, NCI-H69 330527 S77356 transcript ch21 = oligomycin sensitivity c 3.39 NCI-H23, Caco2, A549 8 stomach cancer cell lines, mRNA, 262 n 314660 AA436007 Hs.188780 ESTs 3.39 OVCA-R, BT474, Caco2 321321 AB033072 EST cluster (not in UniGene) 3.39 NCI-358, EB, Caco2 323356 AA234009 Hs.188715 ESTs 3.38 DU145, CALU6, CALU6 328592 CH.07_ha gi|5868227 3.38 MCF7, NCI-358, MB-MDA-231 311116 AI631195 Hs.232193 ESTs 3.36 NCI-H520, NCI-H23, PRSC_log 323853 AA393460 EST cluster (not in UniGene) 3.36 DU145, EB, Caco2 327740 CH.05_hs gi|5867943 3.35 EB, LnCap, OVCA-R 326857 CH.20_hs gi|6552460 3.33 NCI-H69, MCF7, NCI-H345 317787 AW339612 Hs.249364 ESTs 3.31 NCI-H345, PRSC_con, PRSC_log 325760 CH.14_hs gi|6552449 3.3 EB, CALU6, HT29 337513 CH22_FGENES.809-4 3.29 LnCap, NCI-H23, NCI-H460 336606 CH22_FGENES.429_3 3.29 NCI-H69, A549, NCI-H23 322895 AW470295 Hs.192152 ESTs 3.29 DU145, Caco2, EB 314312 AA814971 Hs.257634 ESTs 3.29 RPWE-2, NCI-H69, NCI-H345 328224 CH.06_hs gi|5868101 3.28 DU145, NCI-H345, LnCap 336128 CH22_FGENES.701_16 3.27 BT474, NCI-H520, MB-MDA-231 332442 AA281323 Hs.4947 ESTs 3.27 Caco2, PC3, NCI-H345 302514 M14269 EST cluster (not in UniGene) with exon h 3.27 DU145, CALU6, NCI-H520 313749 AW450376 Hs.130803 ESTs 3.26 OVCA-R, NCI-H69, DU145 302891 AI681578 Hs.114164 ESTs 3.26 LnCap, NCI-H345, PRSC_log 334690 CH22_FGENES.420_3 3.25 NCI-H69, RPWE-2, PRSC_con 308676 AI761036 EST singleton (not in UniGene) with exon 3.25 DU145, MB-MDA-231, HT29 304254 AA046273 Hs.111334 ferritin; light polypeptide 3.24 OVCA-R, DU145, A549 311994 AA648314 Hs.13849 ESTs 3.24 NCI-H460, NCI-H23, MB-MDA-453 321020 AB023170 Hs.227850 KIAA0953 protein 3.24 EB, MCF7, MB-MDA-435s 316724 AA810788 Hs.123337 ESTs 3.23 DU145, OVCA-R, BT474 326942 CH.21_hs gi|6004446 3.22 HT29, BT474, NCI-H23 324824 AI826999 Hs.224624 ESTs 3.21 OVCA-R, MB-MDA-453, EB 320789 R78712 EST cluster (not in UniGene) 3.21 DU145, LnCap, EB 315070 AW131368 Hs.185736 ESTs 3.21 Caco2, NCI-358, NCI-H460 303794 AW241987 Hs.197025 ESTs 3.19 OVCA-R, PC3, LnCap 310237 AI884313 Hs.158906 ESTs 3.19 NCI-358, NCI-H345, MCF7 313960 AA130859 EST cluster (not in UniGene) 3.18 MB-MDA-231, HT29, BT474 336634 CH22_FGENES.13-4 3.18 NCI-H69, NCI-H345, BT474 301085 AA779058 Hs.190428 ESTs; Weakly similar to NG26 [H. sapiens] 3.17 NCI-H345, NCI-H345, NCI-358 313774 AW136836 Hs.144583 ESTs 3.17 Caco2, EB, OVCA-R 307177 AI188864 EST singleton (not in UniGene) with exon 3.17 EB, CALU6, CALU6 324025 AI174861 Hs.190623 ESTs 3.17 OVCA-R, DU145, PC3 313099 AI307359 Hs.128064 ESTs 3.17 MB-MDA-231, BT474, EB 305536 AA770682 EST singleton (not in UniGene) with exon 3.17 NCI-358, Caco2, HT29 331916 AA446131 Hs.124918 ESTs 3.17 EB, OVCA-R, Caco2 314912 AI431345 Hs.161784 ESTs 3.17 EB, BT474, MCF7 303388 AL039604 EST cluster (not in UniGene) with exon h 3.17 HT29, NCI-358, Caco2 332273 R05818 Hs.173830 ESTs 3.16 MCF7, DU145, EB 314697 AW088739 Hs.243770 ESTs 3.16 MB-MDA-453, DU145, MCF7 335344 CH22_FGENES.536_3 3.15 PRSC_log, NCI-H345, PRSC_con 326162 CH.17_hs gi|5867168 3.15 BT474, HT29, HT29 304467 AA424703 EST singleton (not in UniGene) with exon 3.15 NCI-H23, RPWE-2, NCI-H460 339340 CH22_BA354I12.GENSCAN.27-8 3.15 LnCap, OVCA-R, MB-MDA-453 325393 CH.12_hs gi|5866921 3.13 Caco2, NCI-H23, NCI-358 315367 AA732484 Hs.169399 ESTs 3.13 OVCA-R, EB, MB-MDA-453 307085 AI160868 EST singleton (not in UniGene) with exon 3.12 RPWE-2, PRSC_con, PRSC_log 313001 N29264 Hs.249591 ESTs; Moderately similar to !!!! ALU SUB 3.12 NCI-H345, OVCA-R, Caco2 307606 AI290006 EST singleton (not in UniGene) with exon 3.12 MB-MDA-231, HT29, NCI-H23 325710 CH.14_hs gi|6682473 3.09 NCI-H69, MB-MDA-453, BT474 313810 AA400079 Hs.257854 ESTs 3.09 EB, DU145, CALU6 335482 CH22_FGENES.570_11 3.09 NCI-H460, NCI-358, NCI-H23 326310 CH.17_hs gi|5867277 3.08 MCF7, MB-MDA-453, PC3 325742 CH.14_hs gi|6552448 3.08 NCI-H23, NCI-H460, HT29 312467 AI241809 Hs.75458 ribosomal protein L18 3.08 NCI-358, NCI-H23, NCI-H460 327309 CH.01_hs gi|6456757 3.07 NCI-H69, MB-MDA-435s, MB-MDA-435s 310583 AW205632 Hs.211198 ESTs 3.07 OVCA-R, A549, Caco2 322373 W25673 Hs.130829 ESTs 3.07 NCI-H69, PRSC_con, NCI-H345 324497 AW152624 Hs.136340 ESTs 3.06 NCI-H345, RPWE-2, PRSC_con 315095 AA831815 Hs.243788 ESTs 3.06 Caco2, DU145, EB 302445 N79647 EST cluster (not in UniGene) with exon h 3.05 OVCA-R, A549, NCI-H460 302842 AW383226 Hs.163834 ESTs; Highly similar to Chp [R. norvegicu 3.05 A549, DU145, NCI-H23 317346 AA952875 Hs.221274 ESTs 3.04 BT474, HT29, HT29 334650 CH22_FGENES.417_17 3.04 MCF7, BT474, OVCA-R 306644 AI002913 EST singleton (not in UniGene) with exon 3.04 CALU6, MCF7, BT474 322682 AI110679 EST cluster (not in UniGene) 3.03 NCI-H345, RPWE-2, OVCA-R 311065 AW204582 Hs.224906 ESTs 3.03 PRSC_log, PRSC_con, NCI-H460 318623 AA355439 Hs.151547 ESTs 3.03 DU145, MB-MDA-435s, HT29 304978 AA617735 EST singleton (not in UniGene) with exon 3.03 CALU6, BT474, MB-MDA-435s 305554 AA774567 Hs.121774 EST 3.03 EB, NCI-H460, Caco2 302574 U66199 Hs.249165 fibroblast growth factor 11 3.03 HT29, DU145, PC3 336202 CH22_FGENES.719_6 3.02 NCI-H69, NCI-H23, NCI-H23 302893 AL117539 Hs.173515 H sapiens mRNA; cDNA DKFZp586H021 (from 3.02 EB, DU145, CALU6 315166 AI343966 Hs.158528 ESTs 3.01 Caco2, EB, NCI-H69 335606 CH22_FGENES.582_3 3.01 NCI-H23, NCI-H520, NCI-H345 330058 CH.17_p2 gi|6634847 3.01 OVCA-R, HT29, LnCap 303179 AA071215 EST cluster (not in UniGene) with exon h 3.01 MCF7, RPWE-2, MB-MDA-453 307625 AI299617 EST singleton (not in UniGene) with exon 3 MB-MDA-231, LnCap, BT474 323074 AL119445 Hs.203213 ESTs 3 NCI-H23, NCI-H520, NCI-H460 336232 CH22_FGENES.736_7 3 HT29, BT474, MB-MDA-231 334915 CH22_FGENES.457_4 3 NCI-H345, PRSC_con, NCI-H69 329116 CH.X_hs gi|5868650 3 NCI-H69, PRSC_con, RPWE-2 333495 CH22_FGENES.168_5 3 OVCA-R, NCI-H169, NCI-H345 303756 AI738488 Hs.115838 ESTs 2.99 HT29, PRSC_con, DU145 332134 AA610123 Hs.139240 DKFZP564F1422 protein 2.99 EB, A549, MCF7 322916 AW367294 Hs.154091 ESTs 2.99 DU145, DU145, OVCA-R 318050 AI052093 Hs.133132 ESTs 2.99 NCI-H345, DU145, NCI-H520 301019 AI147356 Hs.98722 ESTs 2.99 NCI-358, NCI-H69, MB-MDA-435s 315213 AA587773 Hs.136494 ESTs 2.98 MB-MDA-231, BT474, LnCap 339251 CH22_BA354I12.GENSCAN.7-5 2.98 NCI-H69, PRSC_log, HT29 303835 T05645 EST cluster (not in UniGene) with exon h 2.97 BT474, NCI-H345, LnCap 300070 AI174603 Hs.256832 ESTs 2.97 DU145, A549, OVCA-R 320954 AB028953 Hs.204121 KIAA1030 protein 2.97 LnCap, DU145, PC3 327624 CH.04_hs gi|5867871 2.97 EB, DU145, LnCap 329029 CH.X_hs gi|6525302 2.96 NCI-H69, PRSC_log, LnCap 317040 AA868584 Hs.126154 ESTs 2.96 DU145, EB, LnCap 328016 CH.06_hs gi|5902482 2.96 NCI-H345, PRSC_con, DU145 312674 AI762475 Hs.151327 ESTs; Moderately similar to !!!! ALU SUB 2.96 OVCA-R, NCI-H69, NCI-H69 332301 R70253 Hs.127826 ESTs 2.96 OVCA-R, DU145, MB-MDA-231 300951 AI732374 Hs.105834 ESTs; Weakly similar to 25 kDa trypsin i 2.95 NCI-358, NCI-H460, Caco2 318226 AI078446 Hs.134125 ESTs 2.95 NCI-H460, NCI-H23, NCI-358 311349 AW292933 Hs.254110 ESTs 2.94 EB, DU145, OVCA-R 312757 AI285970 Hs.183817 ESTs 2.94 DU145, LnCap, LnCap 316507 AI381515 Hs.158381 ESTs 2.94 PRSC_con, PRSC_log, RPWE-2 302278 AF018080 Hs.173730 Mediterranean fever 2.93 EB, NCI-H69, DU145 311016 AW173166 Hs.243468 ESTs 2.93 NCI-H345, LnCap, LnCap 323864 AA340724 Hs.214028 ESTs 2.92 EB, Caco2, HT29 336632 CH22_FGENES.13-2 2.92 NCI-H69, NCI-H345, MB-MDA-231 328886 CH.07_hs gi|6588003 2.92 HT29, PC3, LnCap 301859 T61587 EST cluster (not in UniGene) with exon h 2.92 LnCap, EB, EB 323775 AA329856 Hs.143022 ESTs 2.92 PRSC_con, PRSC_log, RPWE-2 315426 AI391486 Hs.128171 ESTs 2.92 CALU6, EB, A549 322264 AF086242 EST cluster (not in UniGene) 2.92 Caco2, OVCA-R, DU145 315135 AA627561 Hs.192446 ESTs 2.91 EB, HT29, DU145 327982 CH.06_hs gi|5868216 2.91 LnCap, MS-MDA-453, NCI-H169 314530 AI052358 Hs.131741 ESTs 2.91 NCI-H460, NCI-H520, RPWE-2 315003 AA527650 Hs.156037 ESTs 2.9 PRSC_con, RPWE-2, MB-MDA-231 339032 CH22_DA59H18.GENSCAN.25-1 2.9 NCI-H69, PRSC_con, RPWE-2 308379 AI623950 Hs.2186 eukaryotic translation elongation factor 2.89 BT474, MB-MDA-231, HT29 312133 T87714 Hs.221665 ESTs 2.88 Caco2, MB-MDA-453, MCF7 307992 AI434166 EST singleton (not in UniGene) with exon 2.88 NCI-H520, MCF7, NCI-H23 308010 AI439190 Hs.181165 eukaryotic translation elongation factor 2.88 Caco2, NCI-H69, NCI-H345 320154 AA336019 Hs.119559 ESTs 2.88 MB-MDA-453, DU145, EB 331496 N34929 Hs.171984 ESTs 2.86 MB-MDA-453, PC3, MCF7 320016 H57622 Hs.194574 ESTs 2.86 PRSC_con, RPWE-2, PRSC_log 317923 AW450544 Hs.220751 ESTs 2.86 NCI-H345, PRSC_con, PRSC_log 301822 X17033 Hs.1142 integrin; alpha 2 (CD49B: alpha 2 subuni 2.86 PC3, BT474, CALU6 311759 AA705075 Hs.169536 Rhesus blood group-associated glycoprote 2.85 DU145, HT29, MB-MDA-231 315083 AI221325 Hs.210655 ESTs 2.84 PRSC_con, RPWE-2, NCI-H345 317759 AI908455 Hs.202460 ESTs; Weakly similar to hypothetical L1 2.83 HT29, MB-MDA-231, BT474 313980 AI633205 Hs.159914 ESTs 2.83 Caco2, MB-MDA-453, A549 310941 AI453402 Hs.173705 ESTs; Weakly similar to !!!! ALU CLASS C 2.83 NCI-H345, MCF7, Caco2 313593 AI911488 Hs.213724 ESTs 2.83 LnCap, Caco2, NCI-H460 314973 AW273128 Hs.254669 EST 2.82 BT474, LnCap, RPWE-2 310950 AI582758 Hs.170561 ESTs 2.82 EB, MB-MDA-453, LnCap 323626 AL039822 Hs.207604 ESTs 2.82 PC3, HT29, CALU6 325410 CH.12_hs gi|5866921 2.81 MB-MDA-453, PRSC_con, NCI-358 313911 AI565458 Hs.116385 ESTs 2.81 PRSC_con, EB, RPWE-2 334244 CH22_GENES.365_5 2.81 OVCA-R, PC3, MB-MDA-453 309333 AW025709 EST singleton (not in UniGene) with exon 2.81 NCI-H460, NCI-H23, NCI-358 328467 CH.07_hs gi|5868434 2.81 EB, OVCA-R, HT29 318563 AW250501 EST cluster (not in UniGene) 2.81 BT474, NCI-H23, MB-MDA-231 326412 CH.19_hs gi|5867362 2.81 BT474, PRSC_log, RPWE-2 303407 AA309616 EST cluster (not in UniGene) with exon h 2.8 CALU6, NCI-H345, DU145 328462 CH.07_hs gi|5868433 2.8 BT474, CALU6, MCF7 335157 CH22_FGENES.501_7 2.8 NCI-H69, NCI-H345, PRSC_log 313458 AA007259 Hs.255853 ESTs 2.79 OVCA-R, DU145, LnCap 310416 AI695047 Hs.202395 ESTs 2.79 DU145, MB-MDA-435s, PC3 317709 AI435973 Hs.128056 ESTs 2.79 NCI-H460, NCI-358, DU145 321415 AI377596 Hs.3337 transmembrane 4 superfamily member 1 2.79 A549, PC3, OVCA-R 313693 AW469180 Hs.170651 ESTs 2.79 OVCA-R, MCF7, EB 309438 AW102802 Hs.225787 ESTs; Moderately similar to hypothetical 2.79 PC3, OVCA-R, DU145 308961 AI870248 EST singleton (not in UniGene) with exon 2.78 BT474, MB-MDA-231, EB 329107 CH.X_hs gi|5868626 2.78 DU145, MCF7, MB-MDA-435s 313975 AW025024 Hs.65114 keratin 18 2.78 Caco2, EB, DU145 330901 AA157818 Hs.238380 Human endogenous retroviral pretease mRN 2.78 PC3, NCI-H520, BT474 311749 R06249 Hs.13911 ESTs 2.78 OVCA-R, MB-MDA-453, MCF7 329853 CH.14_p2 gi|6682295 2.78 BT474, BT474, HT29 322340 AF088076 EST cluster (not in UniGene) 2.77 NCI-H345, Caco2, LnCap 326806 CH.20_hs gi|6469835 2.77 NCI-H69, NCI-H345, MB-MDA-231 314661 AA436432 EST cluster (not in UniGene) 2.77 NCI-H460, MB-MDA-435s, CALU6 322135 AF075082 EST cluster (not in UniGene) 2.77 NCI-358, NCI-H460, Caco2 331849 AA417078 Hs.193767 ESTs 2.77 DU145, EB, CALU6 301056 AI797955 Hs.208076 ESTs; Weakly similar to D(4) DOPAMINE RE 2.76 NCI-H69, RPWE-2, PRSC_con 327739 CH.05_hs gi|5867942 2.76 EB, PC3, LnCap 308016 AI445116 EST singleton (not in UniGene) with exon 2.76 LnCap, HT29, MB-MDA-231 331549 N56866 Hs.237507 EST 2.76 MB-MDA-453, MCF7, OVCA-R 331851 AA418599 Hs.98303 caveolin 3 2.75 MB-MDA-231, NCI-H345, BT474 315023 AA533505 Hs.185844 ESTs 2.75 PRSC_con, OVCA-R, EB 335565 CH22_FGENES.579_1 2.75 OVCA-R, EB, A549 306137 AA916176 EST singleton (not in UniGene) with exon 2.74 EB, LnCap, DU145 332240 N54803 yv31d2.s1 Soares fetal liver spleen 1NFL 2.74 DU145, EB, CALU6 3′ similar to contains L1.t3 L1 repetit 313246 N90762 Hs.159454 ESTs 2.74 NCI-H69, NCI-H345, PRSC_log 303642 AW299459 EST cluster (not in UniGene) with exon h 2.74 EB, A549, Caco2 325513 CH.12_hs gi|6017035 2.74 MB-MDA-231, NCI-H345, BT7474 337236 CH22_FGENES.639-2 2.74 MCF7, MB-MDA-453, NCI-H69 311555 AW407892 Hs.244807 ESTs 2.74 BT474, NCI-H345, NCI-H69 339266 CH22_BA354I12.GENSCAN.10-4 2.73 CALU6, DU145, OVCA-R 300127 AW028615 Hs.235224 ESTs; Weakly similar to KIAA0422 [H. sapi 2.73 NCI-H345, RPWE-2, PRSC_log 311741 R00099 Hs.193642 ESTs 2.72 LnCap, PC3, OVCA-R 310915 AW449673 Hs.201893 ESTs 2.72 DU145, EB, MB-MDA-435s 324982 T31689 Hs.98518 ESTs 2.71 PRSC_con, PRSC_log, RPWE-2 305030 AA629988 EST singleton (not in UniGene) with exon 2.71 DU145, DU145, NCI-358 315396 AW296107 Hs.152686 ESTs 2.69 OVCA-R, Oaco2, EB 319098 AI908374 EST cluster (not in UniGene) 2.69 RPWE-2, LnCap, PC3 309119 AI927384 Hs.228499 EST; Moderately similar to PK-120 precur 2.69 LnCap, NCI-H23, NCI-358 312095 AW444937 Hs.233482 ESTs 2.68 Caco2, OVCA-R, HT29 324316 AI291330 EST cluster (not in UniGene) 2.68 NCI-H460, Caco2, PRSC_log 331367 AA425688 Hs.41641 ESTs; Weakly similar to CAGH4 [H. sapiens 2.68 MB-MDA-435s, NCI-H520, NCI-H460 339116 CH22_DA59H18.GENSCAN.49-4 2.68 DU145, EB, CALU6 324297 AI565566 Hs.168587 ESTs 2.68 PRSC_con, OVCA-R, PRSC_log 318728 Z30201 EST cluster (not in UniGene) 2.68 LnCap, Caco2, PC3 304813 AA584540 EST singleton (not in UniGene) with exon 2.68 BT474, OVCA-R, RPWE-2 312393 N34376 Hs.191659 ESTs; Weakly similar to !!!! ALU CLASS E 2.68 NCI-H345, PRSC_con, EB 330671 AB002302 Hs.92236 KIAA0304 gene product 2.67 NCI-358, OVCA-R, Caco2 305406 AA723860 EST singleton (not in UniGene) with exon 2.66 OVCA-R, EB, MCF7 330957 H08778 Hs.133521 ESTs 2.66 EB, PC3, OVCA-R 300350 AI871129 Hs.172597 ESTs; Weakly similar to zinc finger prot 2.66 NCI-H23, NCI-H520, NCI-H460 322302 W76021 EST cluster (not in UniGene) 2.66 DU145, OVCA-R, PC3 321891 AW157424 Hs.165954 ESTs 2.66 EB, OVCA-R, Caco2 300124 AI217394 Hs.242447 ESTs 2.65 PRSC_con, A549, HT29 302747 AF062275 EST cluster (not in UniGene) with exon h 2.65 NCI-H23, BT474, MCF7 309741 AI802780 Hs.209002 ESTs; Weakly similar to !!!! ALU SUBFAMI 2.65 PC3, EB, OVCA-R 310802 AI631546 Hs.159732 ESTs 2.65 PRSC_con, PRSC_log, NCI-H69 300694 AA063406 EST cluster (not in UniGene) with exon h 2.65 BT474, EB, MCF7 311395 R23313 EST cluster (not in UniGene) 2.64 EB, OVCA-R, DU145 336538 CH22_FGENES.840_2 2.64 DU145, NCI-H460, NCI-358 316473 AA829961 EST cluster (not in UniGene) 2.64 LnCap, OVCA-R, EB 328134 CH.06_hs gi|5868039 2.64 LnCap, EB, CALU6 329330 CH.X_hs gi|5868806 2.64 EB, CALU6, DU145 316664 AI042101 EST cluster (not in UniGene) 2.64 NCI-H345, MB-MDA-231, PRSC_log 328015 CH.06_hs gi|5902482 2.63 BT474, HT29, MB-MDA-231 308991 AI879831 EST singleton (not in UniGene) with exon 2.63 BT474, EB, NCI-H23 323899 AL042966 EST cluster (not in UniGene) 2.62 DU145, A549, CALU6 321708 AA476817 EST cluster (not in UniGene) 2.62 EB, A549, CALU6 301752 T75247 EST cluster (not in UniGene) with exon h 2.62 HT29, BT474, NCI-H345 309351 AW057547 EST singleton (not in UniGene) with exon 2.62 NCI-H23, PRSC_con, LnCap 314412 AI864270 Hs.155654 ESTs 2.62 CALU6, MB-MDA-231, BT474 309441 AW103055 Hs.244230 EST 2.62 BT474, MB-MDA-231, MB-MDA-453 335993 CH22_FGENES.656_6 2.61 NCI-H460, NCI-358, NCI-H520 318196 AI056776 Hs.133397 ESTs 2.6 EB, CALU6, HT29 322880 AA310521 Hs.50848 ESTs; Weakly similar to KIAA0862 protein 2.6 DU145, A549, PC3 300558 AI540051 Hs.122638 ESTs 2.6 OVCA-R, NCI-H69, MCF7 318594 AA918320 Hs.224581 ESTs 2.6 PC3, MB-MDA-453, DU145 308554 AI698132 Hs.201923 EST 2.6 LnCap, EB, NCI-H345 335108 CH22_FGENES.494_14 2.6 NCI-H69, NCI-H345, MB-MDA-231 312483 AI417526 Hs.184636 ESTs 2.59 PC3, DU145, OVCA-R 311981 AW452773 Hs.257612 EST 2.59 NCI-H460, MB-MDA-453, NCI-H23 319359 F13458 EST cluster (not in UniGene) 2.59 LnCap, NCI-H460, MB-MDA-231 300230 AI377746 Hs.158846 ESTs 2.59 HT29, NCI-358, NCI-H345 316504 AW135854 Hs.132458 ESTs 2.59 DU145, EB, CALU6 322337 AA249804 EST cluster (not in UniGene) 2.59 NCI-H69, NCI-H345, NCl-H345 301775 AW247670 EST cluster (not in UniGene) with exon h 2.59 NCI-H345, RPWE-2, PRSC_log 301089 AA666396 Hs.220727 ESTs 2.58 PRSC_log, PRSC_con, RPWE-2 331213 T88698 Hs.163862 ESTs 2.58 DU145, EB, OVCA-R 321121 W23285 EST cluster (not in UniGene) 2.58 NCI-H69, MB-MDA-435s, PC3 316634 AW241910 Hs.122254 ESTs 2.58 MCF7, HT29, BT474 322141 AF075092 EST cluster (not in UniGene) 2.58 PC3, OVCA-R, HT29 312108 T82331 Hs.127453 ESTs 2.58 A549, CALU6, Caco2 339071 CH22_DA59H18.GENSCAN.34-1 2.58 CALU6, DU145, EB 311666 AW389509 Hs.223747 ESTs 2.57 OVCA-R, MB-MDA-231, BT474 318662 AI285898 Hs.115367 ESTs 2.57 OVCA-R, DU145, EB 317010 AA863395 EST cluster (not in UniGene) 2.57 NCI-H520, PRSC_con, NCI-358 324710 AI742028 Hs.120884 ESTs; Weakly similar to RAS-RELATED PROT 2.57 LnCap, DU145, MB-MDA-453 327888 CH.06_hs gi|5868149 2.56 NCI-H345, MB-MDA-435s, RPWE-2 336149 CH22_FGENES.706.5 2.56 NCI-H69, PC3, A549 312816 H74319 Hs.188620 ESTs 2.56 EB, Caco2, NCI-H460 327999 CH.06_hs gi|5867994 2.56 NCI-358, NCI-H520, NCI-H23 316761 AI911173 Hs.213722 ESTs 2.55 NCI-H345, NCI-H460, MB-MDA-231 336958 CH22_FGENES.367-1 2.55 HT29, CALU6, CALU6 325043 W27919 Hs.32944 inositol polyphosphate-4-phosphatase; ty 2.55 NCI-H460, NCI-H23, HT29 315417 AW452360 Hs.186770 ESTs 2.55 NCI-H345, NCI-H69, PRSC_con 331603 N78656 Hs.161535 EST 2.55 NCI-H345, PRSC_con, PRSC_log 309403 AW082954 EST singleton (not in UniGene) with exon 2.55 BT474, MB-MDA-231, MCF7 337289 CH22_FGENES.672-8 2.54 BT474, HT29, MB-MDA-231 314242 AI570943 Hs.246280 ESTs 2.54 Caco2, MB-MDA-435s, MB-MDA-453 328053 CH.06_hs gi|5902482 2.54 MB-MDA-231, DU145, MB-MDA-453 307215 AI193189 EST singleton (not in UniGene) with exon 2.53 HT29, CALU6, MB-MDA-231 327566 CH.03_hs gi|5867811 2.53 NCI-H69, NCI-H520, NCI-H345 326338 CH.17_hs gi|6056311 2.53 PC3, A549, DU145 318115 AI384027 Hs.159130 ESTs; Moderately similar to !!!! ALU SUB 2.53 DU145, EB, PC3 307437 AI245683 EST singleton (not in UniGene) with exon 2.52 NCI-H23, NCI-H520, NCI-358 322059 AA412371 Hs.121344 ESTs 2.52 EB, DU145, OVCA-R 322505 AF147315 EST cluster (not in UniGene) 2.52 PRSC_con, RPWE-2, NCI-H69 314032 AW081897 Hs.193211 ESTs 2.52 NCI-H345, LnCap, DU145 336125 CH22_FGENES.701_12 2.51 NCI-H69, LnCap, DU145 312765 AI692908 Hs.181873 ESTs 2.51 NCI-H23, NCI-358, NCI-H520 335523 CH22_FGENES.572_3 2.51 HT29, BT474, OVCA-R 327585 CH.03_hs gi|5867825 2.51 HT29, NCI-H460, MB-MDA-453 323183 AW393850 EST cluster (not in UniGene) 2.51 MB-MDA-231, LnCap, RPWE-2 314418 AI478722 Hs.232275 ESTs; Moderately similar to !!!! ALU SUB 2.51 EB, DU145, DU145 313361 AI359782 Hs.137312 ESTs 2.5 CALU6, HT29, DU145 305632 AA805276 EST singleton (not in UniGene) with exon 2.5 MB-MDA-453, NCI-H460, NCI-H23 331689 W90131 Hs.184675 ESTs 2.5 NCI-H69, EB, A549 323438 AI540243 Hs.113817 ESTs 2.5 NCI-H345, PRSC_con, MB-MDA-231 315742 AI821724 Hs.143198 H sapiens PAC clone DJ0872F07 from 7q31 2.5 MCF7, MB-MDA-453, MB-MDA-435s 305971 AA886874 EST singleton (not in UniGene) with exon 2.5 NCI-358, NCI-H23, NCI-H520 336633 CH22_FGENES.13-3 2.5 NCI-H69, NCI-H345, PRSC_log 304746 AA577793 EST singleton (not in UniGene) with exon 2.49 NCI-H69, BT474, MB-MDA-231 327925 CH.06_hs gi|5868172 2.49 NCI-358, NCI-358, NCI-H460 336055 CH22_FGENES.683_4 2.49 EB, HT29, MB-MDA-231 328888 CH.07_hs gi|6588003 2.48 MB-MDA-435s, MB-MDA-453, PRSC_log 311244 AW016694 Hs.197689 ESTs 2.48 NCI-H345, MCF7, PC3 327155 CH.01_hs gi|5867549 2.48 NCI-H69, MB-MDA-231, NCI-H345 334907 CH22_FGENES.453_2 2.48 DU145, NCI-H345, MB-MDA-231 314887 AA910236 Hs.139469 ESTs 2.48 DU145, A549, A549 339435 CH22_DJ579N16.GENSCAN.18-10 2.48 NCI-H69, MCF7, BT474 334172 CH22_FGENES.349_5 2.48 NCI-H69, NCI-H345, PRSC_log 320767 AA299525 EST cluster (not in UniGene) 2.48 NCI-358, NCI-H23, NCI-H460 338772 CH22_FGENES.156-1 2.47 NCI-358, NCI-358, NCI-H23 326957 CH.21_hs gi|6469836 2.47 BT474, RPWE-2, PRSC_con 308505 AI686615 Hs.200778 EST; Weakly similar to SALIVARY PROLINE- 2.47 MCF7, MB-MDA-453, MB-MDA-435s 321325 AB033100 EST cluster (not in UniGene) 2.47 EB, CALU6, A549 313149 AW291092 Hs.201058 ESTs 2.47 NCI-H345, PRSC_con, RPWE-2 338325 CH22_EM:AC005500.GENSCAN.307-7 2.46 BT474, LnCap, EB 307877 AI368880 EST singleton (not in UniGene) with exon 2.46 NCI-H23, PRSC_log, NCI-H520 311525 AI799444 Hs.247095 ESTs; Moderately similar to !!!! ALU SUB 2.46 PRSC_con, PRSC_log, NCI-H345 337023 CH22_FGENES.433-12 2.46 OVCA-R, CALU6, PRSC_con 300916 AI361798 Hs.164675 ESTs 2.45 LnCap, DU145, CALU6 302919 AL137382 EST cluster (not in UniGene) with exon h 2.45 LnCap, MB-MDA-231, CALU6 320303 AL079289 Hs.137154 H sapiens mRNA full length insert cDNA c 2.45 BT474, MB-MDA-231, MB-MDA-453 318359 AI097439 Hs.135548 ESTs 2.45 NCI-H460, MB-MDA-453, NCI-H345 314384 AA535840 Hs.162203 ESTs; Weakly similar to altematively sp 2.45 OVCA-R, PC3, EB 326763 CH.20_hs gi|6598307 2.45 NCI-H69, NCI-H345, RPWE-2 319900 AW408392 EST cluster (not in UniGene) 2.45 Caco2, NCI-H460, NCI-H23 314451 AA586368 Hs.190232 ESTs 2.45 PRSC_con, NCI-H345, MB-MDA-231 300641 AW237699 Hs.118346 ESTs 2.44 NCI-H345, PRSC_log, PRSC_con 324368 AW299374 EST cluster (not in UniGene) 2.44 PC3, DU145, OVCA-R 336510 CH22_FGENES.834_5 2.44 NCI-H69, RPWE-2, PRSC_con 326876 CH.20_hs gi|6682507 2.44 NCI-H23, NCI-H460, NCI-H520 307753 AI340509 Hs.182426 ribosomal protein S2 2.44 NCI-H23, NCI-H460, Caco2 317071 M78728 Hs.132694 ESTs 2.44 NCI-H345, NCI-H69, RPWE-2 313877 AA767869 Hs.250113 ESTs; Moderately similar to thyroid horm 2.44 DU145, LnCap, CALU6 component TRAP150 [H. sapiens] 315974 AW029203 Hs.191952 ESTs 2.43 EB, DU145, OVCA-R 322970 AI885052 Hs.142287 ESTs; Weakly similar to !!!! ALU CLASS F 2.43 NCI-H345, RPWE-2, EB 317733 AI028257 Hs.132317 ESTs 2.43 CALU6, RPWE-2, OVCA-R 313599 AA748749 Hs.136742 ESTs 2.42 NCI-H460, NCI-358, NCI-H520 323014 AA305198 EST cluster (not in UniGene) 2.42 PRSC_con, NCI-H460, RPWE-2 324980 AA969121 Hs.254296 ESTs 2.41 MCF7, OVCA-R, PC3 301326 AA883831 Hs.252924 ESTs 2.41 PRSC_con, PRSC_log, RPWE-2 308695 AI763350 EST singleton (not in UniGene) with exon 2.41 RPWE-2, NCI-H69, NCI-H345 330166 CH.02_p2 gi|6648220 2.41 CALU6, DU145, A549 317552 AW451400 Hs.127019 ESTs 2.41 NCI-358, NCI-358, NCI-H23 320572 AI929508 Hs.159590 lymphocyte antigen 6 complex; locus H 2.41 CALU6, HT29, A549 315618 AI287341 Hs.154029 ESTs; Weakly similar to TRANSCRIPTION FA 2.41 OVCA-R, Caco2, MB-MDA-231 331610 N91109 Hs.54681 ESTs 2.41 NCI-H23, NCI-H520, NCI-358 311731 AW393528 Hs.246875 ESTs 2.41 NCI-H69, NCI-H345, PRSC_con 318571 Z43383 Hs.8053 ESTs 2.4 NCI-358, NCI-H23, NCI-H520 334958 CH22_FGENES.465_27 2.4 DU145, PRSC_con, RPWE-2 323570 AL038623 Hs.208752 ESTs; Weakly similar to !!!! ALU SUBFAMI 2.4 OVCA-R, EB, BT474 301685 W67730 EST cluster (not in UniGene) with exon h 2.4 MB-MDA-231, NCI-H345, EB 303849 AW163324 EST cluster (not in UniGene) with exon h 2.4 RPWE-2, PRSC_log, NCI-H345 325702 CH.14_hs gi|5867028 2.4 NCI-H23, NCI-H460, NCI-H520 313074 N48261 Hs.127171 ESTs 2.4 MB-MDA-231, RPWE-2, PRSC_log 308994 AI880051 EST singleton (not in UniGene) with exon 2.4 RPWE-2, EB, PRSC_con 330338 CH.08_p2 gi|5457162 2.4 DU145, EB, LnCap 327274 CH.01_hs gi|5867470 2.4 OVCA-R, DU145, MB-MDA-231 325953 CH.16_hs gi|5867140 2.4 MB-MDA-453, MB-MDA-435s, MCF7 333281 CH22_FGENES.128_7 2.4 NCI-H23, HT29, DU145 314778 AW079559 Hs.152258 ESTs 2.39 EB, CALU6, Caco2 317005 AI800251 Hs.197773 ESTs 2.38 MB-MDA-231, BT474, HT29 334257 CH22_FGENES.367_5 2.38 HT29, NCI-358, MB-MDA-231 324783 AA640770 EST cluster (not in UniGene) 2.38 EB, OVCA-R, MB-MDA-453 300949 AA534325 Hs.162183 ESTs 2.38 NCI-H69, NCI-H345, PRSC_log 314957 AW029274 Hs.208368 ESTs; Moderately similar to !!!! ALU SUB 2.38 LnCap, DU145, DU145 324350 AW292501 Hs.157174 ESTs; Weakly similar to similar to SH3-b 2.38 HT29, NCI-H23, NCI-H23 338235 CH22_EM:AC005500.GENSCAN.260-16 2.38 NCI-H69, NCI-H460, NCI-H23 300937 AW297302 Hs.255631 ESTs 2.38 PRSC_log, PRSC_con, PRSC_con 317439 AW451327 Hs.170623 ESTs 2.38 A549, DU145, EB 324745 AI742120 Hs.116506 ESTs; Weakly similar to !!!! ALU SUBFAMI 2.38 NCI-358, NCI-H460, BT474 338306 CH22_EM:AC005500.GENSCAN.302-2 2.38 NCI-H69, PRSC_con, PRSC_log 318765 Z42071 Hs.23961 ESTs 2.38 LnCap, NCI-H23, NCI-H520 310254 AI239811 Hs.157491 ESTs 2.37 OVCA-R, DU145, EB 305116 AA649244 EST singleton (not in UniGene) with exon 2.37 CALU6, MB-MDA-435s, MB-MDA-453 324016 AL045285 Hs.245849 ESTs; Moderately similar to !!!! ALU SUB 2.37 EB, DU145, OVCA-R 322774 AA131111 EST cluster (not in UniGene) 2.37 OVCA-R, EB, A549 335745 CH22_FGENES.601_16 2.37 PRSC_log, PRSC_con, NCI-H69 300972 AI979100 Hs.211518 ESTs 2.37 NCI-H69, NCI-H345, PRSC_log 338809 CH22_EMAC005500.GENSCAN.531-10 2.37 NCI-H23, NCI-H69, NCI-H520 316983 AI480204 Hs.177131 ESTs 2.37 NCI-H345, PRSC_con, PRSC_log 321308 AI247480 Hs.117029 ESTs 2.37 BT474, NCI-H69, HT29 323578 AA299492 Hs.168166 ESTs 2.37 LnCap, EB, MB-MDA-453 335747 CH22_FGENES.601_20 2.36 NCI-H69, LnCap, PRSC_con 322362 AF039697 EST cluster (not in UniGene) 2.36 DU145, PRSC_con, NCI-H345 314430 N76302 Hs.78110 ESTs; Weakly similar to F17A9.2 [C. elega 2.36 DU145, MB-MDA-453, CALU6 304831 AA586422 EST singleton (not in UniGene) with exon 2.36 NCI-H23, NCI-H460, CALU6 337432 CH22_FGENES.765-1 2.36 MB-MDA-231, BT474, HT29 305984 AA887654 EST singleton (not in UniGene) with exon 2.36 DU145, HT29, CALU6 313486 AW134523 Hs.247186 ESTs 2.36 DU145, A549, CALU6 309028 AI889109 Hs.212032 EST 2.36 NCI-358, NCI-H520, NCI-H23 318292 AI679966 Hs.150603 ESTs 2.35 NCI-H460, Caco2, NCI-H23 334198 CH22_FGENES.354_4 2.35 NCI-H69, PRSC_log, PRSC_con 314458 AI217440 Hs.143873 ESTs 2.35 Caco2, A549, PC3 333346 CH22_FGENES.139_15 2.35 CALU6, DU145, LnCap 325408 CH.12_hs gi|5866921 2.35 NCI-H460, NCI-H520, NCI-H23 313758 AA076743 Hs.129770 ESTs 2.35 NCI-H23, MB-MDA-435s, NCI-H345 309825 AW293701 EST singleton (not in UniGene) with exon 2.35 NCI-H460, NCI-H23, NCI-H520 303536 R55497 Hs.183941 ESTs; Moderately similar to H beta 58 ho 2.35 DU145, CALU6, NCI-H520 331534 N51583 Hs.133756 EST 2.35 NCI-H23, NCI-H520, NCI-358 325164 T16981 Hs.21963 ESTs 2.34 NCI-H345, PRSC_log, NCI-H460 327710 CH.04_hs gi|5867860 2.34 BT474, MB-MDA-231, NCI-H345 306351 AA961356 EST singleton (not in UniGene) with exon 2.34 BT474, MB-MDA-231, MB-MDA-435s 304968 AA614308 EST singleton (not in UniGene) with exon 2.34 CALU6, HT29, MB-MDA-453 334015 CH22_FGENES.313_7 2.34 HT29, MB-MDA-231, BT474 318315 AI091370 Hs.134852 ESTs 2.33 CALU6, NCI-H520, DU145 306809 AI057134 EST singleton (not in UniGene) with exon 2.33 PC3, DU145, EB 337697 CH22_EM:AC000097.GENSCAN.86-1 2.33 RPWE-2, PRSC_log, NCI-H345 329630 CH.11_p2 gi|6729060 2.33 NCI-H520, NCI-H23, NCI-H460 326577 CH.19_hs gi|5867317 2.33 NCI-H460, NCI-358, NCI-H23 333428 CH22_FGENES.149_1 2.33 NCI-H345, PRSC_con, RPWE-2 301080 AI479391 Hs.155405 ESTs; Weakly similar to !!!! ALU SUBFAMI 2.33 OVCA-R, MCF7, MCF7 324829 AA714311 EST cluster (not in UniGene) 2.33 NCI-H460, NCI-358, NCI-H23 302776 AJ133798 EST cluster (not in UniGene) with exon h 2.32 NCI-H23, NCI-H460, NCI-H520 325801 CH.14_hs gi|6552451 2.32 PRSC_log, MCF7, NCI-H23 332122 AA609698 Hs.112389 ESTs 2.32 DU145, HT29, PC3 314167 AA243633 Hs.208983 ESTs 2.32 DU145, MCF7, PC3 324023 AA669615 Hs.214226 ESTs 2.31 DU145, NCI-H345, EB 320503 NM_00589 EST cluster (not in UniGene) 2.31 A549, OVCA-R, PC3 312217 T98289 EST cluster (not in UniGene) 2.31 NCI-H23, Caco2, NCI-H69 321304 AA078293 EST cluster (not in UniGene) 2.31 DU145, OVCA-R, EB 323517 AA527359 Hs.154366 ESTs 2.31 NCI-H345, DU145, EB 336455 CH22_FGENES.829_13 2.31 NCI-H345, PRSC_con, RPWE-2 313352 AW292127 Hs.144758 ESTs 2.31 MCF7, DU145, OVCA-R 331457 H93135 Hs.41840 ESTs 2.31 Caco2, NCI-H460, NCI-H23 333054 CH22_FGENES.73_8 2.31 NCI-H69, NCI-358, NCI-H23 308598 AI719237 EST singleton (not in UniGene) with exon 2.31 OVCA-R, CALU6, Caco2 327059 CH.21_hs gi|6531965 2.3 NCI-H460, LnCap, LnCap 334120 CH22_FGENES.333_1 2.3 NCI-H69, RPWE-2, MB-MDA-435s 324154 AI457449 Hs.192817 ESTs 2.3 NCI-H460, MB-MDA-453, NCI-358 326509 CH.19_hs gi|6682496 2.3 NCI-H345, CALU6, OVCA-R 316855 AW291384 Hs.254974 ESTs 2.3 NCI-H345, NCI-H460, BT474 337918 CH22_EM:AC005500.GENSCAN.66-4 2.3 RPWE-2, NCI-H345, PRSC_log 317471 AI825351 Hs.144084 ESTs 2.29 HT29, OVCA-R, DU145 331023 N32599 Hs.5856 ESTs 2.29 OVCA-R, LnCap, A549 332231 N48008 Hs.102629 EST 2.29 CALU6, DU145, EB 309912 AW339671 EST singleton (not in UniGene) with exon 2.29 MB-MDA-435s, PRSC_con, NCI-358 316427 AI241019 Hs.145644 ESTs 2.29 Caco2, HT29, EB 313329 AW293704 Hs.122658 ESTs 2.29 OVCA-R, DU145, Caco2 335019 CH22_FGENES.474_7 2.29 HT29, CALU6, MB-MDA-231 324394 F20654 Hs.152128 ESTs; Moderately similar to !!!! ALU SUB 2.29 NCI-H345, MB-MDA-231, RPWE-2 339357 CH22_BA354|12.GENSCAN.31-2 2.29 NCI-H69, OVCA-R, BT474 322128 AI346033 EST cluster (not in UniGene) 2.28 NCI-H23, NCI-H520, NCI-H460 301310 AI239457 Hs.130794 ESTs 2.28 OVCA-R, DU145, MB-MDA-231 300623 AI929130 Hs.118261 ESTs; Moderately similar to finger prote 2.28 BT474, RPWE-2, PRSC_con 323409 AL135534 EST cluster (not in UniGene) 2.27 NCI-H345, NCI-358, Caco2 308406 AI634885 EST singleton (not in UniGene) with exon 2.27 OVCA-R, EB, HT29 322518 AI133446 EST cluster (not in UniGene) 2.27 DU145, MB-MDA-435s, OVCA-R 338381 CH22_EM:AC005500.GENSCAN.330-10 2.27 NCI-H69, PRSC_con, PRSC_log 316003 AA704584 Hs.119993 ESTs 2.27 NCI-358, NCI-H520, NCI-H23 307090 AI161024 EST singleton (not in UniGene) with exon 2.27 NCI-H345, DU145, RPWE-2 300356 AA758411 Hs.121335 ESTs 2.27 LnCap, NCI-H460, Caco2 331887 AA431328 Hs.98660 ESTs 2.27 NCI-358, NCI-H520, CALU6 330951 H02566 Hs.191268 H sapiens mRNA; cDNA DKFZp434N174 (from 2.27 OVCA-R, BT474, BT474 305547 AA773111 EST singleton (not in UniGene) with exon 2.27 LnCap, DU145, BT474 312457 AA776743 Hs.191589 ESTs 2.26 NCI-H345, RPWE-2, PRSC_con 333929 CH22_FGENES.300_2 2.26 HT29, CALU6, EB 319845 AA649011 Hs.187902 ESTs 2.26 LnCap, DU145, MCF7 306739 AI028393 EST singleton (not in UniGene) with exon 2.26 MB-MDA-435s, NCI-358, CALU6 306919 AI096832 EST singleton (not in UniGene) with exon 2.26 HT29, BT474, PC3 333312 CH22_FGENES.138_4 2.26 OVCA-R, DU145, PC3 334955 CH22_FGENES.465_24 2.25 RPWE-2, PRSC_con, NCI-H345 312295 AA578233 Hs.173863 ESTs 2.25 OVCA-R, DU145, NCI-H345 307643 AI302124 EST singleton (not in UniGene) with exon 2.25 CALU6, CALU6, OVCA-R 324252 AA421989 EST cluster (not in UniGene) 2.25 OVCA-R, EB, A549 309767 AW271805 EST singleton (not in UniGene) with exon 2.25 DU145, NCI-H460, CALU6 311492 AW410240 Hs.4437 ribosomal protein L28 2.25 NCI-H69, NCI-H460, NCI-H520 312260 H05392 Hs.230597 EST 2.25 Caco2, EB, DU145 327125 CH.21_hs gi|6531971 2.25 HT29, NCI-358, BT474 316919 AA845382 Hs.204520 ESTs 2.24 NCI-H23, NCI-H345, NCI-H520 316361 AI433833 Hs.164159 ESTs; Weakly similar to !!!! ALU SUBFAMI 2.24 DU145, EB, PC3 315772 AW515373 Hs.158893 ESTs 2.24 OVCA-R, EB, LnCap 320236 H03688 EST cluster (not in UniGene) 2.24 NCI-358, DU145, NCI-H23 315444 AW138821 Hs.221737 ESTs 2.24 NCI-358, CALU6, PRSC_con 333903 CH22_FGENES.294_1 2.24 MB-MDA-231, BT474, A549 335234 CH22_FGENES.515_3 2.24 NCI-H69, PRSC_con, PRSC_log 333727 CH22_FGENES.256_1 2.23 MB-MDA-231, NCI-H69, BT474 332002 AA482009 Hs.105104 ESTs 2.23 EB, NCI-H520, HT29 329611 CH.10_p2 gi|3962478 2.23 BT474, HT29, MB-MDA-231 310559 AI783594 Hs.155718 ESTs 2.22 BT474, MCF7, MB-MDA-231 327315 CH.01_hs gi|5867508 2.22 NCI-H69, EB, EB 323170 U83527 EST cluster (not in UniGene) 2.22 EB, DU145, LnCap 331522 N49309 Hs.117012 ESTs 2.22 A549, LnCap, DU145 313261 AA730472 Hs.142805 ESTs 2.22 OVCA-R, PC3, LnCap 312740 R97191 Hs.134106 ESTs 2.22 BT474, MCF7, OVCA-R 325055 Z44631 Hs.21658 ESTs 2.22 MB-MDA-453, DU145, CALU6 337895 CH22_EM:AC005500.GENSCAN.56-2 2.22 NCI-H345, PRSC_log, PRSC_con 307140 AI185762 EST singleton (not in UniGene) with exon 2.22 NCI-H520, NCI-H460, EB 321643 W76005 Hs.32094 ESTs 2.21 EB, NCI-H345, PRSC_con 302683 X85153 EST cluster (not in UniGene) with exon h 2.21 BT474, MB-MDA-231, MCF7 322644 AA340904 EST cluster (not in UniGene) 2.21 NCI-H460, NCI-H23, NCI-H520 330415 D83777 Hs.75137 KIAA0193 gene product 2.21 CALU6, A549, Caco2 302334 AF120491 EST cluster (not in UniGene) with exon h 2.21 NCI-H69, NCI-H345, PC3 326710 CH.20_hs gi|5867593 2.21 NCI-H520, NCI-358, NCI-H23 323561 AA825426 Hs.238832 ESTs; Weakly similar to !!!! ALU SUBFAMI 2.21 NCI-H345, DU145, NCI-H69 337706 CH22_EM:AC000097.GENSCAN.87-11 2.21 MB-MDA-435s, NCI-358, NCI-H520 339309 CH22_BA354I12.GENSCAN.22-7 2.21 BT474, HT29, PC3 330436 HG2724-H Oncogene Tls/Chop, Fusion Activated 2.21 PRSC_con, NCI-H69, Caco2 312360 AI922972 Hs.196073 ESTs 2.21 OVCA-R, MB-MDA-435s, DU145 301855 AF053356 multiple UniGene matches 2.2 NCI-H69, HT29, NCI-H23 331192 T55182 Hs.152571 ESTs; Highly similar to IGF-II mRNA-bind 2.2 OVCA-R, PC3, CALU6 315872 AW051819 Hs.204516 ESTs 2.2 LnCap, OVCA-R, EB 337904 CH22_EM:AC005500.GENSCAN.56-17 2.2 OVCA-R, LnCap, EB 308258 AI565612 EST singleton (not in UniGene) with exon 2.2 DU145, MB-MDA-231, CALU6 320965 H18166 EST cluster (not in UniGene) 2.2 DU145, EB, LnCap 333910 CH22_FGENES.295_3 2.2 DU145, MB-MDA-231, EB 300707 AA080921 EST cluster (not in UniGene) with exon h 2.2 BT474, MCF7, HT29 336011 CH22_FGENES.668_9 2.19 NCI-H460, BT474, NCI-H345 325712 CH.14_hs gi|6682473 2.19 NCI-H460, NCI-H23, NCI-358 322738 AF201832 EST cluster (not in UniGene) 2.19 PC3, RPWE-2, PRSC_con 335339 CH22_FGENES.535_16 2.19 HT29, PRSC_log, MCF7 320733 AA738436 Hs.134407 ESTs 2.19 DU145, EB, Caco2 319412 AA679426 Hs.187505 ESTs 2.19 NCI-H345, PRSC_log, PRSC_con 337132 CH22_FGENES.526-3 2.19 NCI-H69, NCI-H345, PRSC_con 301544 AI951651 Hs.224290 ESTs 2.19 PRSC_con, MB-MDA-231, NCI-H23 325285 CH.11_hs gi|5866903 2.18 PRSC_con, PRSC_log, MB-MDA-231 338280 CH22_EM:AC005500.GENSCAN.290-11 2.18 PC3, NCI-358, HT29 311421 AI701635 Hs.207077 ESTs 2.18 RPWE-2, NCI-H345, NCI-358 330638 X89576 Hs.159581 matrix metalloproteinase 17 (membrane-in 2.18 HT29, MB-MDA-435s, MB-MDA-453 326603 CH.20_hs gi|6056312 2.18 CALU6, DU145, HT29 319055 AA412305 EST cluster (not in UniGene) 2.18 A549, OVCA-R, MB-MDA-435s 335451 CH22_FGENES.562_9 2.18 DU145, LnCap, CALU6 317989 AI203009 Hs.130664 ESTs 2.18 NCI-H345, NCI-H69, NCI-H520 322024 AA334384 EST cluster (not in UniGene) 2.18 Caco2, PC3, NCI-H520 300734 AW205197 Hs.240951 ESTs 2.18 NCI-358, A549, EB 304022 T02990 EST singleton (not in UniGene) with exon 2.18 NCI-H23, NCI-358, NCI-H460 330082 CH.19_p2 gi|6015314 2.18 NCI-H23, Caco2, Caco2 312516 AA363245 Hs.189831 ESTs 2.18 BT474, HT29, MB-MDA-231 333932 CH22_FGENES.300_5 2.17 PC3, Caco2, EB 308115 AI479071 EST singleton (not in UniGene) with exon 2.17 BT474, OVCA-R, OVCA-R 320184 U91510 Hs.123036 CD39-like 1 2.17 NCI-H520, NCI-358, NCI-H23 324432 AA464510 EST cluster (not in UniGene) 2.17 CALU6, RPWE-2, HT29 320882 AI832098 EST cluster (not in UniGene) 2.17 OVCA-R, PC3, BT474 312251 H03952 EST cluster (not in UniGene) 2.17 NCI-H460, NCI-H23, NCI-358 315049 AW340486 Hs.121210 ESTs 2.17 NCI-H520, NCI-358, NCI-H23 305018 AA627127 EST singleton (not in UniGene) with exon 2.17 MB-MDA-231, MB-MDA-453, EB 303807 AI792785 Hs.130434 ESTs 2.16 NCI-H345, PRSC_con, PRSC_log 317792 AI653389 Hs.196121 ESTs 2.16 NCI-H345, PRSC_con, LnCap 321668 AA872730 Hs.125229 ESTs 2.16 OVCA-R, PC3, MCF7 328863 CH.07_hs gi|6381929 2.16 PRSC_con, NCI-H345, NCI-H460 319373 R00371 EST cluster (not in UniGene) 2.16 PRSC_con, RPWE-2, NCI-H345 320069 T86541 Hs.189732 ESTs 2.16 NCI-H23, NCI-358, NCI-H345 320235 AF064090 Hs.129708 tumor necrosis factor (ligand) superfami 2.16 NCI-H23, NCI-8460, NCI-H520 338880 CH22_DJ32I10.GENSCAN.6-2 2.16 BT474, MCF7, OVCA-R 318314 AI091349 Hs.161133 ESTs 2.16 NCI-H23, NCI-H520, NCI-H460 332696 D86973 Hs.75354 GCN1 (general control of amino-acid synt 2.16 A549, PC3, DU145 331352 AA406133 Hs.7482 KIAA0682 gene product 2.16 PC3, EB, MB-MDA-231 339019 CH22_DA59H18.GENSCAN.21-15 2.15 LnCap, EB, OVCA-R 306975 AI127042 EST singleton (not in UniGene) with exon 2.15 MB-MDA-435s, NCI-H520, NCI-358 318069 AI024557 Hs.131540 ESTs 2.15 Caco2, Caco2, BT474 312997 AW205686 Hs.135130 ESTs 2.15 NCI-H460, NCI-H23, NCI-358 331372 AA433935 Hs.55044 DKFZP586H2123 protein 2.15 PRSC_con, HT29, CALU6 335049 CH22_FGENES.481_5 2.15 NCI-H69, NCI-H345, PRSC_log 324280 AA429772 Hs.191610 ESTs 2.15 MB-MDA-453, MB-MDA-435s, MCF7 330363 CH.X_p2 gi|3126882 2.15 NCI-H23, NCI-H460, NCI-358 322896 AW470296 Hs.144830 ESTs 2.15 HT29, CALU6, EB 321981 AA948204 Hs.127361 ESTs 2.15 MB-MDA-231, DU145, HT29 333294 CH22_FGENES.130_6 2.14 EB, DU145, MB-MDA-453 330170 CH.02_p2 gi|6648220 2.14 HT29, MB-MDA-453, PC3 312973 AI123346 Hs.135241 ESTs 2.14 LnCap, DU145, EB 311104 AI627352 Hs.201449 ESTs 2.14 NCI-H520, NCI-H23, LnCap 325086 T10019 Hs.4194 ESTs 2.14 NCI-H460, NCI-H23, NCI-358 317182 AW183524 Hs.192298 ESTs 2.14 HT29, BT474, MB-MDA-435s 323644 AA310711 Hs.124340 ESTs 2.14 RPWE-2, PRSC_con, PRSC_log 308092 AI474896 EST singleton (not in UniGene) with exon 2.14 BT474, MCF7, MB-MDA-231 322265 AF086244 EST cluster (not in UniGene) 2.14 NCI-H345, RPWE-2, PRSC_con 303521 AA746272 EST cluster (not in UniGene) with exon h 2.14 DU145, MB-MDA-453, EB 312102 AW439340 Hs.189720 ESTs 2.14 NCI-H23, NCI-H460, MB-MDA-435s 316559 AI249468 Hs.228251 EST 2.14 NCI-H460, NCI-358, NCI-H23 338486 CH22_EM:AC005500.GENSCAN.382-8 2.14 NCI-H520, NCI-H23, NCI-H69 301302 AI825444 Hs.210956 ESTs 2.14 BT474, HT29, MB-MDA-231 310591 AI650372 Hs.195979 ESTs 2.14 CALU6, CALU6, Caco2 316231 AA732301 EST cluster (not in UniGene) 2.14 NCI-H23, NCI-H520, NCI-358 326559 CH.19_hs gi|5867310 2.14 DU145, NCI-H460, NCI-H23 324062 AA525291 Hs.204099 ESTs; Weakly similar to !!!! ALU SUBFAMI 2.13 OVCA-R, DU145, EB 323844 AI811303 Hs.143490 ESTs 2.13 MB-MDA-453, MCF7, MB-MDA-435s 333895 CH22_FGENES.293_2 2.13 CALU6, LnCap, DU145 308264 AI567114 Hs.171454 EST 2.13 DU145, CALU6, MB-MDA-453 306081 AA908472 EST singleton (not in UniGene) with exon 2.13 HT29, 6T474, MB-MDA-231 333101 CH22_FGENES.79_6 2.13 NCI-H345, NCI-H69, PRSC_log 328544 CH.07_hs gi|5868486 2.13 NCI-H23, NCI-H69, PRSC_log 333355 CH22_.FGENES.141_6 2.13 DU145, EB, CALU6 323397 AI524519 Hs.239699 ESTs 2.13 EB, NCI-H460, NCI-H345 305697 AA814956 EST singleton (not in UniGene) with exon 2.13 NCI-H520, NCI-H460, NCI-358 327809 CH.05_hs gi|5867968 2.13 HT29, PC3, OVCA-R 325092 T10115 Hs.92423 ESTs 2.13 HT29, NCI-358, MB-MDA-231 322299 AI971935 Hs.252784 ESTs 2.13 PRSC_con, DU145, DU145 312145 AA029526 Hs.126706 ESTs 2.12 OVCA-R, A549, MB-MDA-435s 323704 AA319421 Hs.193577 ESTs 2.12 Caco2, LnCap, OVCA-R 328971 CH.08_hs gi|6478806 2.12 NCI-358, NCI-H23, NCI-H520 325338 CH.11_hs gi|5866883 2.12 LnCap, NCI-H69, NCI-H345 331332 AA282554 Hs.89034 ESTs 2.12 NCI-H520, NCI-H23, Caco2 327159 CH.01_hs gi|5867550 2.12 EB, DU145, PC3 335180 CH22_FGENES.505_2 2.12 LnCap, NCI-H69, A549 338062 CH22_EM:AC005500.GENSCAN.162-3 2.12 PRSC_con, PRSC_log, NCI-H69 318350 AI636018 Hs.135538 ESTs 2.12 EB, HT29, DU145 312070 AW293140 Hs.108790 ESTs 2.11 Caco2, NCI-H23, A549 328314 CH.07_hs gi|5868371 2.11 HT29, NCI-H23, NCI-H460 315869 AI033547 Hs.132826 ESTs 2.11 BT474, CALU6, MCF7 339246 CH22_BA354|12.GENSCAN.5-9 2.11 CALU6, CALU6, BT474 329921 CH.16_p2 gi|6165205 2.11 BT474, MB-MDA-231, HT29 324981 Z25333 Hs.4947 ESTs 2.11 A549, NCI-H460, NCI-H520 331291 AAI59323 Hs.109929 ESTs 2.11 NCI-H345, A549, PRSC_con 332729 AA058907 Hs.83190 fatty acid synthase 2.11 NCI-358, LnCap, MB-MDA-453 325448 CH.12_hs gi|5866941 2.11 DU145, MCF7, CALU6 314929 AW188286 Hs.143612 ESTs 2.1 EB, BT474, MB-MDA-231 301063 AI057634 Hs.124596 ESTs 2.1 NCI-H23, NCI-H460, BT474 301952 A5029016 Hs.117333 KIAA1093 protein 2.1 OVCA-R, A549, CALU6 326309 CH.17_hs gi|5867277 2.1 MB-MDA-435s, NCI-H69, MB-MDA-453 315406 AI823453 Hs.146625 ESTs 2.1 OVCA-R, DU145, EB 302376 AB007867 Hs.200480 KIAA0407 protein 2.1 OVCA-R, Caco2, HT29 312181 AA417281 Hs.191595 ESTs 2.1 OVCA-R, A549, DU145 334254 CH22_FGENES.366_4 2.1 LnCap, OVCA-R, DU145 318073 AW167087 Hs.131562 ESTs 2.1 A549, CALU6, EB 304724 AA569881 Hs.65114 keratin 18 2.1 NCI-H23, NCI-H520, NCI-H460 332359 W87704 Hs.211558 ESTs 2.1 MB-MDA-435s, PRSC_con, NCI-H460 331884 AA431302 Hs.98721 EST: Weakly similar to N-copine [H. sapie 2.1 NCI-H345, MB-MDA-231, PRSC_con 308226 AI559106 Hs.181165 eukaryotic translation elongation factor 2.1 EB, CALU6, OVCA-R 324279 AA501412 Hs.191688 ESTs; Weakly similar to Pro-Pol-dUTPase 2.09 OVCA-R, LnCap, PC3 337203 CH22_.FGENES.591-3 2.09 NCI-H69, NCI-H345, MB-MDA-231 322346 AA227618 Hs.10882 HMG-box containing protein 1 2.09 HT29, BT474, MB-MDA-231 304470 AA426654 Hs.195188 glyceraldehyde-3-phosphate dehydrogenase 2.09 NCI-H23, CALU6, NCI-H520 325977 CH.16_hs gi|6249602 2.09 NCI-H23, NCI-H520, HT29 304696 AA554758 EST singleton (not in UniGene) with exon 2.09 MB-MDA-435s, NCI-H23, BT474 317412 AI301528 Hs.132604 ESTs 2.09 Caco2, EB, NCI-358 315570 AI860360 Hs.160316 ESTs 2.08 PRSC_con, PRSC_log, NCI-H345 327341 CH.01_hs gi|6017016 2.08 MB-MDA-231, PRSC_con, NCI-H69 327431 CH.02_hs gi|5867754 2.08 NCI-H23, NCI-358, NCI-H520 314685 AI870811 Hs.158709 ESTs; Weakly similar to KIAA0938 protein 2.08 MB-MDA-453, MCF7, OVCA-R 328624 CH.07_hs gi|5868246 2.08 MCF7, NCI-358, RPWE-2 303596 AW303377 EST cluster (not in UniGene) with exon h 2.08 RPWE-2, PRSC_con, PRSC_log 336717 CH22_FGENES.81-1 2.08 BT474, HT29, MCF7 317370 AW204139 Hs.174424 ESTs; Weakly similar to p140mDia [M. musc 2.08 NCI-H23, NCI-H460, NCI-H69 331287 AA149061 Hs.172971 ESTs 2.08 OVCA-R, EB, NCI-H345 304211 N62228 EST singleton (not in UniGene) with exon 2.08 BT474, MCF7, MB-MDA-231 315613 AW137420 Hs.192311 ESTs 2.08 PRSC_con, PRSC_log, PRSC_log 325636 CH.14_hs gi|5867002 2.08 NCI-358, NCI-H460, MB-MDA-453 336406 CH22_FGENES.823_21 2.08 HT29, EB, DU145 301714 F06529 EST cluster (not in UniGene) with exon h 2.08 LnCap, PRSC_log, PRSC_con 300496 R45159 Hs.221804 ESTs 2.08 PRSC_con, LnCap, RPWE-2 318970 R21114 Hs.21383 ESTs 2.08 NCI-H23, NCI-H520, NCI-H460 334115 CH22_FGENES.330_115 2.08 BT474, NCI-H69, HT29 308082 AI473682 EST singleton (not in UniGene) with exon 2.08 MB-MDA-435s, NCI-H345, MB-MDA-231 308282 AI569456 EST singleton (not in UniGene) with exon 2.08 LnCap, EB, PRSC_con 313038 AW451618 Hs.124195 ESTs 2.07 NCI-H345, PRSC_con, LnCap 317974 AW444468 Hs.144900 ESTs 2.07 NCI-358, NCI-H23, NCI-H520 324063 AW292740 Hs.254815 ESTs 2.07 Caco2, NCI-358, NCI-H520 334759 CH22_FGENES.428_8 2.07 CALU6, HT29, NCI-H520 307864 AI367417 EST singleton (not in UniGene) with exon 2.07 NCI-H460, NCI-358, NCI-H423 304356 AA196027 Hs.195188 glyceraldehyde-3-phosphate dehydrogenase 2.07 HT29, MCF7, MB-MDA-435s 303929 AW470753 EST singleton (not in UniGene) with exon 2.07 NCI-H345, PRSC_con, RPWE-2 331857 AA421160 Hs.9456 SWI/SNF related; matrix assocd; actin de 2.07 EB, A549, PC3 322814 AI824495 Hs.211038 ESTs 2.06 PRSC_con, RPWE-2, Caco2 303650 AA430709 EST cluster (not in UniGene) with exon h 2.06 RPWE-2, NCI-H345, PRSC_con 333403 CH22_FGENES.144_21 2.06 OVCA-R, CALU6, PC3 313663 AI953261 Hs.169813 ESTs 2.06 NCI-H345, OVCA-R, NCI-H23 338594 CH22_EM:AC005500.GENSCAN.435-4 2.06 DU145, LnCap, EB 334676 CH22_FGENES.418_29 2.06 NCI-H69, PRSC_log, PRSC_con 310046 AI198032 Hs.210356 ESTs 2.06 MB-MDA-435s, NCI-H23, Caco2 309169 AI949216 EST singleton (not in UniGene) with exon 2.06 CALU6, EB, NCI-358 329752 CH.14_p2 gi|6065777 2.06 CALU6, HT29, DU145 325085 T10001 Hs.4188 ESTs 2.06 EB, OVCA-R, MB-MDA-435s 332062 AA521016 Hs.185375 ESTs 2.06 OVCA-R, MB-MDA-453, MCF7 302074 AA382871 Hs.132794 phosphate cytidylyltransferase 1; cholin 2.06 LnCap, EB, NCI-H69 326344 CH.17_hs gi|6525295 2.06 HT29, BT474, MB-MDA-453 330855 AA079318 zm98c2.s1 Stratagene colon HT29 (#937221 2.06 RPWE-2, LnCap, PRSC_con IMAGE:545954 3′, mRNA seq 302525 AF024690 Hs.248056 G protein-coupled receptor 43 2.05 NCI-358, NCI-H23, DU145 331903 AA436673 Hs.29417 H sapiens mRNA; cDNA DKFZp586B0323 2.05 Caco2, DU145, A549 (from 316322 AW296618 Hs.120637 ESTs 2.05 BT474, MB-MDA-453, OVCA-R 321525 H78875 EST cluster (not in UniGene) 2.05 NCI-H23, PRSC_con, NCI-H520 305071 AA640579 EST singleton (not in UniGene) with exon 2.05 MB-MDA-231, BT474, HT29 326033 CH.17_hs gi|5867178 2.05 HT29, DU145, BT474 334730 CH22_FGENES.424_5 2.05 BT474, EB, OVCA-R 305335 AA704235 EST singleton (not in UniGene) with exon 2.05 MCF7, OVCA-R, MB-MDA-453 320521 N31464 Hs.24743 ESTs 2.05 MB-MDA-453, MB-MDA-231, PC3 333515 CH22_FGENES.172_5 2.04 NCI-H345, RPWE-2, PRSC_con 311020 AI918672 Hs.213783 ESTs 2.04 NCI-H460, NCI-H23, NCI-H520 324323 AA393739 EST cluster (not in UniGene) 2.04 OVCA-R, PC3, LnCap 305486 AA748889 EST singleton (not in UniGene) with exon 2.04 NCI-H345, PRSC_log, CALU6 312162 T91823 EST cluster (not in UniGene) 2.04 NCI-H520, NCI-H23, NCI-358 330980 H28794 Hs.6659 ESTs 2.04 MCF7, MB-MDA-453, MB-MDA-435s 317463 AA927290 Hs.130462 ESTs 2.04 NCI-H23, Caco2, NCI-H69 303460 AA700155 Hs.117900 ESTs 2.04 DU145, EB, CALU6 337435 CH22_FGENES.766-2 2.03 NCI-H345, OVCA-R, LnCap 305464 AA742425 EST singleton (not in UniGene) with exon 2.03 CALU6, NCI-H520, NCI-358 307918 AI383496 EST singleton (not in UniGene) with exon 2.03 NCI-H23, BT474, MB-MDA-231 322209 H89360 EST cluster (not in UniGene) 2.03 DU145, OVCA-R, MB-MDA-453 310295 AW205198 Hs.149146 ESTs 2.03 NCI-H23, NCI-H460, NCI-358 325886 CH.16_hs gi|5867087 2.03 NCI-H345, NCI-H345, RPWE-2 329719 CH.14_.p2 gi|6065785 2.03 NCI-H69, RPWE-2, PRSC_con 309247 AI972768 EST singleton (not in UniGene) with exon 2.03 LnCap, PRSC_con, RPWE-2 328277 CH.07_hs gi|6004471 2.03 LnCap, RPWE-2, A549 307296 AI205705 Hs.147222 EST 2.03 NCI-H460, NCI-358, NCI-H23 327203 CH.01_hs gi|5867447 2.03 HT29, BT474, MB-MDA-231 306866 AI086683 EST singleton (not in UniGene) with exon 2.03 BT474, NCI-H345, HT29 333339 CH22_FGENES.139_8 2.03 HT29, DU145, CALU6 323115 AI921875 EST cluster (not in UniGene) 2.03 BT474, BT474, MB-MDA-231 304811 AA584361 EST singleton (not in UniGene) with exon 2.03 NCI-H23, NCI-358, NCI-H460 323372 AL135125 Hs.13913 ESTs 2.02 DU145, EB, A549 312854 AA828713 EST cluster (not in UniGene) 2.02 NCI-H345, PRSC_con, PRSC_log 307904 AI381019 EST singleton (not in UniGene) with exon 2.02 HT29, MCF7, MB-MDA-453 332099 AA608983 afsd4.s1 Soares_testis_NHT H sapiens cDN 2.02 PRSC_con, NCI-H345, RPWE-2 324634 AI684571 Hs.175831 ESTs 2.02 NCI-H460, Caco2, NCI-358 335721 CH22_FGENES.599_24 2.02 NCI-H69, PRSC_log, NCI-H345 312452 AI692643 Hs.172749 ESTs 2.02 HT29, Caco2, MB-MDA-231 325396 CH.12_hs gi|5866921 2.01 HT29, NCI-H520, NCI-H450 328770 CH.07_hs gi|6017031 2.01 NCI-H23, NCI-H460, NCI-358 335585 CH22_FGENES.581_24 2.01 MB-MDA-453, DU145, MCF7 335634 CH22_FGENES.584_14 2.01 NCI-H23, NCI-H460, NCI-H69 338271 CH22_EM:AC005500.GENSCAN.287-1 2.01 MCF7, DU145, PC3 328607 CH.07_hs gi|5868233 2.01 NCI-H460, NCI-H23, NCI-358 307050 AI147341 Hs.146734 EST 2.01 NCI-H520, NCI-H23, NCI-358 334946 CH22_FGENES.465_13 2.01 CALU6, BT474, DU145 319793 R56360 EST cluster (not in UniGene) 2.01 NCI-H460, HT29, NCI-358 307223 AI193698 Hs.184776 ribosomal protein L23a 2.01 NCI-358, NCI-H520, NCI-H23 312627 AA344698 Hs.133169 ESTs 2.01 PC3, LnCap, MB-MDA-231 329221 CH.X_hs gi|5868727 2.01 NCI-H345, NCI-H69, NCI-358 305145 AA653589 EST singleton (not in UniGene) with exon 2.01 LnCap, EB, OVCA-R 328428 CH.07_hs gi|5868417 2.01 NCI-H69, MB-MDA-453, BT474 305990 AA888866 Hs.125919 EST 2.01 NCI-H520, NCI-358, NCI-H23 319368 R00003 Hs.133171 ESTs 2 OVCA-R, LnCap, PC3 324805 AA927002 Hs.131350 ESTs 2 NCI-H460, NCI-H23, NCI-358 301138 AA719179 Hs.189419 ESTs 2 NCI-H69, NCI-H23, PRSC_con 304675 AA541740 EST singleton (not in UniGene) with exon 2 NCI-H460, NCI-H520, MB-MDA-231 326194 CH.17_hs gi|5867213 2 HT29, NCI-358, 87474

[0331] TABLE 5 H chip - B survivor vs Met query - up in Mets Pkey Ex Accn UniG_ID Complete_Title Ratio Met/B surv. 102193 U20758 Hs. 313 secreted phosphoprotein 1 (osteopontin; 5.56 128530 AA504343 Hs. 183475 Homo sapiens clone 25061 mRNA sequence 4.62 129093 AA262710 Hs. 108614 KIAA0627 protein 4.23 124690 R05818 Hs. 173830 ESTs 3.96 115558 AA393806 Hs. 1010 regulator of mitotic spindle assembly 1 3.39 134261 AA227678 Hs. 8084 Humn DNA sequence from clone 465N24 on c 3.22 104792 AA029288 Hs. 29147 ESTs; Highly similar to ZINC FINGER PROT 3.17 133770 M69197 Hs. 242279 haptoglobin-related protein 3.07

[0332] TABLE 6 H chip - B survivor vs Met query - down in Mets Pkey Ex Accn UniG_ID Complete_Title Ratio Met/B surv. 100116 D00654 Hs. 77443 actin; gamma 2; smooth muscle; enteric 0.07 101923 S75256 HNL = neutrophil lipocalin [human, ovarian 0.2 129982 M87789 Hs. 140 immunoglobulin gamma 3 (Gm marker) 0.2 130064 T67053 Hs. 181125 immunoglobulin lambda gene cluster 0.2

[0333] TABLE 7 I chip - B survivor vs Met query - up in Mets Pkey Ex_Accn UniG_ID Title Ratio Met/B surv 319379 T91443 Hs. 193963 ESTs 19.65 321920 N63915 11.9 324302 AA543008 Hs. 136806 ESTs; Weakly similar to !!!! ALU SUBFAMI 9.31 314522 AI732331 Hs. 187750 ESTs; Moderately similar to !!!! ALU CLA 5.79 331433 H68097 Hs. 161023 EST 4.79 324643 AI436356 Hs. 130729 ESTs 4.59 332471 AA416967 Hs. 120980 nuclear receptor co-repressor 2 4.58 314915 AA573072 Hs. 187748 ESTs; Weakly similar to !!!! ALU SUBFAMI 4.3 321354 AA078493 EST cluster (not in UniGene) 4.26 322309 AF086372 EST cluster (not in UniGene) 3.89 325100 T10265 Hs. 116122 ESTs; Weakly similar to coded for by C. 3.81 314071 AA192455 Hs. 188690 ESTs 3.74 315178 AW362945 Hs. 162459 ESTs 3.66 330987 H40988 Hs. 131965 ESTs; Weakly similar to !!!! ALU SUBFAMI 3.51 337898 CH22_EM: AC005500.GENSCAN.56-5 3.21 319403 T98413 EST cluster (not in UniGene) 3.2 331469 N22273 Hs. 39140 ESTs 3.15 331549 N56866 Hs. 237507 EST 3.14 331644 T99544 Hs. 173734 ESTs; Weakly similar to !!!! ALU CLASS B 3.14 313220 AI971981 Hs. 118241 ESTs 3.04

[0334] TABLE 8 I chip - B survivor vs Met query - down in Mets Pkey Ex_Accn UniG_ID Title Ratio Met/B surv 333658 CH22_FGENES.241_4 0.06 333657 CH22_FGENES.241_2 0.07 333654 CH22_FGENES.240_2 0.07 332859 CH22_FGENES.27_2 0.07 333656 CH22_FGENES.240_4 0.07 304480 AA430373 EST singleton (not in UniGene) with exon 0.08 333737 CH22_FGENES.261_1 0.09 308601 AI719930 EST singleton (not in UniGene) with exon 0.1 334030 CH22_FGENES.320_2 0.1 333637 CH22_FGENES.229_2 0.13 302347 AF039400 Hs. 194659 chloride channel; calcium activated; fam 0.16 333653 CH22_FGENES.239_2 0.16 333635 CH22_FGENES.228_2 0.19 333647 CH22_FGENES.235_2 0.19 307588 AI285535 EST singleton (not in UniGene) with exon 0.2 337954 CH22_EM: AC005500.GENSCAN.96-3 0.2 333588 CH22_FGENES.206_2 0.21 320244 AA296922 Hs. 129778 gastrointestinal peptide 0.22 333642 CH22_FGENES.231_2 0.23 337951 CH22_EM: AC005500.GENSCAN.94-1 0.23 333730 CH22_FGENES.258_1 0.23 333646 CH22_FGENES.234_2 0.24

[0335] TABLE 9 H chip - B survivor vs Met query - up in Mets Median Mets AI vs Pkey Ex Accn UniGID Complete_Title Median B-Sur AI 100655 HG2841-HT2970 Albumin, Alt. Splice 5 11.98 124875 R70506 Hs. 207693 ESTs; Weakly similar to !!!! ALU SUBFAMI 9.21 102193 U20758 Hs. 313 secreted phosphoprotein 1 (osteopontin; 6.73 100654 HG2841-HT2969 Albumin, Alt. Splice 3, Missplicing In Alloalbumin Venezia 6.18 118828 N79496 Hs. 50824 EST 5.93 128046 AA873285 Hs. 137947 ESTs 5.9 128896 D14446 Hs. 107 fibrinogen-like 1 5.17 127917 AA211895 Hs. 118831 EST; Highly similar to dJ1163J1.2.1 [H.s 5.11 125090 T91518 ye20f05.s1 Stratagene lung (#937210) Hom 4.47 118579 N68905 small inducible cytokine A5 (RANTES) 4.23 123526 AA608657 ESTs; Moderately similar to !!!! ALU SUB 4.21 128062 AA379500 Hs. 193155 ESTs 4.14 119174 R71234 yi54c08.s1 Soares placenta Nb2HP Homo sa 4.11 128530 AA504343 Hs. 183475 Homo sapiens clone 25061 mRNA sequence 4.09 119404 T92950 ye27c10.s1 Stratagene lung (#937210) Hom 3.98 118475 N66845 Hs. 165411 ESTs; Weakly similar to !!!! ALU CLASS B 3.96 129974 K00629 Hs. 199300 Human kpni repeat mma (cdna clone pcd-k 3.87 108888 AA135606 Hs. 189384 ESTs; Weakly similar to !!!! ALU SUBFAMI 3.85 123963 C13961 Hs. 210115 EST 3.8 123523 AA608588 Hs. 193634 ESTs 3.76 128230 AA984074 Hs. 176757 ESTs 3.75 124090 H09570 Hs. 143032 ESTs; Weakly similar to neuronal thread 3.67 124690 R05818 Hs. 173830 ESTs 3.58 134261 AA227678 Hs. 8084 Human DNA sequence from clone 465N24 on 3.57 126917 AA176225 Hs. 193929 ESTs 3.52 126050 H27267 Hs. 75860 hydroxyacyl-Coenzyme A dehydrogenase/3-k 3.45 126649 AA856990 Hs. 125058 ESTs 3.42 115096 AA255991 Hs. 175319 ESTs 3.4 129906 H39216 Hs. 239970 ESTs; Weakly similar to ZNF91L [H.sapien 3.38 123022 AA480909 aa28f10.s1 NCI_CGAP_GCB1 Homo sapiens cD 3.38 106145 AA424791 Hs. 5734 KIAA0679 protein 3.38 125191 W67257 Hs. 138871 ESTs; Weakly similar to !!!! ALU CLASS B 3.36 108836 AA132061 Hs. 222727 ESTs; Weakly similar to ubiquitous TPR m 3.3 128710 J04813 Hs. 104117 cytochrome P450; subfamily IIIA (niphedi 3.27 123460 AA598981 Hs. 251122 EST 3.25 133735 AC002045 Hs. 251928 nuclear pore complex interacting protein 3.24 124696 R06273 Hs. 186467 ESTs; Moderately similar to !!!! ALU SUB 3.24 120748 AA303153 Hs. 237994 EST; Weakly similar to !!!! ALU SUBFAMIL 3.21 133770 M69197 Hs. 242279 haptoglobin-related protein 3.17 128336 AI242720 Hs. 146043 ESTs; Weakly similar to alternatively sp 3.14 135357 AA235803 Hs. 79572 cathepsin D (lysosomal aspartyl protease 3.12 128088 R02443 Hs. 186467 ESTs; Moderately similar to !!!! ALU SUB 3.08 124055 F10904 Hs. 100516 Homo sapiens clone 23605 mRNA sequence 3.06 124896 R82063 Hs. 101594 EST 3.06 127598 AA610677 Hs. 168851 ESTs 3.04 116802 H44061 Hs. 194026 ESTs 3.01

[0336] TABLE 10 H chip - B survivor vs Met query - Down in Mets Pkey Ex Accn UniG_ID Complete_Title Ratio Met/B surv. 100116 D00654 Hs. 77443 actin; gamma 2; smooth muscle; enteric 0.09 130064 T67053 Hs. 181125 immunoglobulin lambda gene cluster 0.11 129982 M87789 Hs. 140 immunoglobulin gamma 3 (Gm marker) 0.12 131219 C00476 Hs. 24395 small inducible cytokine subfamily B (Cy 0.13 133806 M12759 Hs. 76325 Human Ig J chain gene 0.17 132982 L02326 Hs. 198118 immunoglobulin lambda-like polypeptide 2 0.18 131713 X57809 Hs. 181125 immunoglobulin lambda gene cluster 0.18 131791 S71043 Hs. 32225 immunoglobulin alpha 1 0.2 133725 V00563 Hs. 179543 immunoglobulin mu 0.22 101923 S75256 HNL = neutrophil lipocalin [human, ovarian 0.23 101461 M22430 Hs. 76422 phospholipase A2; group IIA (platelets; 0.24 103448 X99133 Hs. 204238 lipocalin 2 (oncogene 24p3) 0.24

[0337] TABLE 11 H chip - Met vs Normal query - up in Mets Median Mets Al vs Pkey Ex Accn UniG_ID Complete_Title Median Normal Al 100655 HG2841-HT2970 Albumin, Alt. Splice 5 15.91 102193 U20758 Hs. 313 secreted phosphoprotein 1 (osteopontin; 6.83 124875 R70506 Hs. 207693 ESTs; Weakly similar to !!!! ALU SUBFAMI 6.68 100654 HG2841-HT2969 Albumin, Alt. Splice 3, Missplicing In Alloalbumin Venezia 5.28 124059 F13673 Hs. 99769 ESTs 5.11 128896 D14446 Hs. 107 fibrinogen-like 1 5.05 134453 X70683 Hs. 83484 SRY (sex determining region Y)-box 4 4.82 131564 AA491465 Hs. 28792 ESTs 4.78 127917 AA211895 Hs. 118831 EST; Highly similar to dJ1163J1.2.1 [H.s 4.76 115096 AA255991 Hs. 175319 ESTs 4.67 104558 R56678 Hs. 88959 Human DNA sequence from clone 967N21 on 4.63 123526 AA608657 ESTs; Moderately similar to !!!! ALU SUB 4.61 125090 T91518 ye20f05.s1 Stratagene lung (#937210) Hom 4.59 129666 M77349 Hs. 118787 transforming growth factor, beta-induced 4.58 118828 N79496 Hs. 50824 EST 4.56 128046 AA873285 Hs. 137947 ESTs 4.45 133421 AA436560 Hs. 7327 claudin 1 4.09 129158 J05257 Hs. 109 dipeptidase 1 (renal) 4.04 128062 AA379500 Hs. 193155 ESTs 4.03 124696 R06273 Hs. 186467 ESTs; Moderately similar to !!!! ALU SUB 4.01 118475 N66845 Hs. 165411 ESTs; Weakly similar to !!!! ALU CLASS B 3.96 104755 AA024482 Hs. 9029 DKFZP434G032 protein 3.83 104978 AA088458 Hs. 19322 ESTs 3.74 118579 N68905 small inducible cytokine A5 (RANTES) 3.7 123796 AA620390 Hs. 247444 ESTs 3.62 127240 AA888387 Hs. 243845 ESTs; Moderately similar to !!!! ALU SUB 3.61 104105 AA422123 Hs. 42457 ESTs 3.55 129349 D86974 Hs. 110613 KIAA0220 protein 3.54 119329 T51832 ESTs; Moderately similar to !!!! ALU SUB 3.53 114617 AA084148 Hs. 110659 ESTs 3.52 123143 AA487595 aa95e2.s1 Stratagene fetal retina 93722 3.48 103119 X63629 Hs. 2877 cadherin 3; P-cadherin (placental) 3.48 119404 T92950 ye27c10.s1 Stratagene lung (#937210) Hom 3.47 123963 C13961 Hs. 210115 EST 3.47 116480 C14088 Hs. 195188 glyceraldehyde-3-phosphate dehydrogenase 3.4 108836 AA132061 Hs. 222727 ESTs; Weakly similar to ubiquitous TPR m 3.39 120748 AA303153 Hs. 237994 EST; Weakly similar to !!!! ALU SUBFAMIL 3.38 133770 M69197 Hs. 242279 haptoglobin-related protein 3.38 132358 X60486 Hs. 46423 H4 histone family; member G 3.37 127759 AI369384 arylsulfatase D 3.37 129095 L12350 Hs. 108623 thrombospondin 2 3.37 128261 AI061213 Hs. 13179 ESTs; Moderately similar to !!!! ALU SUB 3.36 126908 AA169866 ESTs; Weakly similar to !!!! ALU SUBFAMI 3.36 128954 N32118 Hs. 209100 DKFZP434C171 protein 3.34 119174 R71234 yi54c08.s1 Soares placenta Nb2HP Homo sa 3.33 106687 AA463234 Hs. 119387 KIAA0792 gene product 3.32 128230 AA984074 Hs. 176757 ESTs 3.3 126649 AA856990 Hs. 125058 ESTs 3.25 124620 N74051 Hs. 194092 ESTs; Weakly similar to !!!! ALU SUBFAMI 3.24 135427 AFFX control: human alu repeats 3.23 129967 H99653 Hs. 138618 ESTs 3.22 125191 W67257 Hs. 138871 ESTs; Weakly similar to !!!! ALU CLASS B 3.2 124684 R02401 Hs. 221078 ESTs 3.2 128010 AA856953 Hs. 23348 S-phase kinase-associated protein 2 (p45 3.17 119423 T99544 Hs. 173734 ESTs; Weakly similar to !!!! ALU CLASS B 3.16 123022 AA480909 aa28f10.s1 NCI_CGAP_GCB1 Homo sapiens cD 3.15 103654 Z70759 H. sapiens mitochondrial 16S rRNA gene (p 3.13 128336 AI242720 Hs. 146043 ESTs; Weakly similar to alternatively sp 3.12 124690 R05818 Hs. 173830 ESTs 3.1 129791 F02778 Hs. 173887 KIAA0876 protein 3.07 114472 AA028924 Hs. 177407 ESTs; Weakly similar to !!!! ALU SUBFAMI 3.07 115429 AA284139 Hs. 89295 EST 3.06 130020 AA433930 Hs. 240443 ESTs; Weakly similar to !!!! HNK-1 sulfotrans 3.06 126050 H27267 Hs. 75860 hydroxyacyl-Coenzyme A dehydrogenase/3-k 3.05 129906 H39216 Hs. 239970 ESTs; Weakly similar to ZNF91L [H.sapien 3.04 123422 AA598484 Hs. 238476 EST 3.03 103059 X57351 Hs. 174195 interferon induced transmembrane protein 3.02 124253 H69742 Hs. 102201 ESTs 3.02 123523 AA608588 Hs. 193634 ESTs 3.02 132669 AA188378 Hs. 54602 ESTs; Weakly similar to 60S RIBOSOMAL PR 3.02 123196 AA489250 Hs. 59403 serine palmitoyltransferase; subunit II 3.01 122948 AA477483 zu44h2.s1 Soares ovary tumor NbHOT Homo 3.01 119053 R11501 yf28f1.s1 Soares fetal liver spleen 1NFL 3.01 125953 H40829 yo05d11.r1 Soares adult brain N2b5HB55Y 3 119155 R61715 Hs. 138237 ESTs 3

[0338] TABLE 12 H chip - Met vs Normal query - down in Mets Pkey Ex Accn UniG_ID Complete_Title Median Mets Al vs Median Normal Al 103466 Y00339 Hs. 155097 carbonic anhydrase II 0.01 104258 AF007216 Hs. 5462 solute carrier family 4; sodium bicarbon 0.02 108999 AA156064 Hs. 72115 ESTs 0.04 101046 K01160 Accession not listed in Genbank 0.04 133565 H57056 Hs. 204831 ESTs 0.05 101346 L76465 Hs. 77348 hydroxyprostaglandin dehydrogenase 15-(N 0.05 123137 AA487468 Hs. 100686 ESTs; Weakly similar to secreted cement 0.05 134534 X73501 Hs. 84905 H. Sapiens mRNA for cytokeratin 20 0.05 118823 N79237 Hs. 50813 ESTs; Weakly similar to long chain fatty 0.06 102095 U11313 Hs. 75760 sterol carrier protein 2 0.06 111855 R37362 Hs. 21351 ESTs 0.06 129105 AA224351 Hs. 108681 ESTs 0.07 130320 U19495 Hs. 237356 stromal cell-derived factor 1 0.07 113778 W15263 Hs. 5422 ESTs 0.07 116786 H25836 Hs. 83429 tumor necrosis factor (ligand) superfami 0.07 100116 D00654 Hs. 77443 actin; gamma 2; smooth muscle; enteric 0.07 104636 AA004415 Hs. 106106 ESTs 0.07 107032 AA599472 Hs. 247309 succinate-CoA ligase; GDP-forming; beta 0.08 106605 AA457718 Hs. 21103 Homo sapiens mRNA; cDNA DKFZp564B076 (fr 0.08 128906 AA487557 Hs. 10706 ESTs 0.08 130016 AA055811 Hs. 143131 transmembrane glycoprotein 0.08 113523 T90037 Hs. 16686 ESTs 0.08 102638 U67319 Hs. 9216 caspase 7; apoptosis-related cysteine pr 0.09 124308 H93575 Hs. 227146 Homo sapiens mRNA; cDNA DKFZp564J142 (fr 0.09 129519 AA298786 Hs. 112242 ESTs 0.09 134749 L10955 Hs. 89485 carbonic anhydrase IV 0.09 130366 L11708 Hs. 155109 hydroxysteroid (17-beta) dehydrogenase 2 0.09 109272 AA195718 Hs. 86030 ESTs 0.09 102124 U14528 Hs. 29981 solute carrier family 26 (sulfate transp 0.1 132711 N73702 Hs. 238927 ESTs 0.1 131861 D11925 Hs. 184245 KIAA0929 protein Msx2 interacting nuclea 0.1 133806 M12759 Hs. 76325 Human Ig J chain gene 0.1 102571 U60115 Homo sapiens skeletal muscle LIM-protein 0.1 114846 AA234929 Hs. 44343 ESTs 0.11 131328 V01512 Hs. 25647 v-fos FBJ murine osteosarcoma viral onco 0.11 106569 AA455983 Hs. 117816 sorcin 0.11 103542 Z11793 Hs. 3314 selenoprotein P; plasma; 1 0.11 128915 C02386 Hs. 107139 ESTs 0.11 120914 AA377254 Hs. 97107 EST 0.11 130867 J04093 Hs. 2056 UDP glycosyltransferase 1 0.11 110837 N30796 Hs. 17424 ESTs; Weakly similar to semaphorin F [H. 0.12 101877 M97496 Hs. 778 guanylate cyclase activator 1B (retina) 0.12 132617 AA171913 Hs. 5338 carbonic anhydrase XII 0.12 129113 AA147646 Hs. 108740 DKFZP586A0522 protein 0.12 133435 T23983 Hs. 7365 ESTs 0.13 132836 F09557 Hs. 57929 slit (Drosophila) homolog 3 0.13 125832 AA628600 Hs. 117587 ESTs 0.13 104613 AA001049 Hs. 24713 Homo sapiens mRNA; cDNA DKFZp586G0123 (f 0.13 132903 AA235404 Hs. 5985 Homo sapiens clone 25186 mRNA sequence 0.13 119479 W32094 Hs. 55501 ESTs 0.14 131273 AA421139 Hs. 173542 ESTs 0.14 106674 AA461303 Hs. 7946 DKFZP586D1519 protein 0.14 108980 AA151676 Hs. 33455 peptidyl arginine deiminase; type II 0.14 103211 X73079 Hs. 205126 polymeric immunoglobulin receptor 0.14 131219 C00476 Hs. 24395 small inducible cytokine subfamily B (Cy 0.15 116459 AA621399 Hs. 64193 ESTs 0.15 130219 R77539 Hs. 15285 ESTs 0.15 113863 W68388 Hs. 21288 ESTs; Weakly similar to KIAA0704 protein 0.15 101564 M32886 Hs. 117816 sorcin 0.15 109502 AA233837 Hs. 44755 ESTs; Weakly similar to membrane glycopr 0.15 107222 D51235 Hs. 82689 tumor rejection antigen (gp96) 1 0.15 135237 AA454930 Hs. 9691 ESTs 0.15 112483 R66534 Hs. 28403 ESTs 0.15 132387 R70914 Hs. 8997 heat shock 70 kD protein 1 0.15 130343 AA490262 Hs. 15485 ESTs; Weakly similar to APICAL-LIKE PROT 0.16 105496 AA256323 Hs. 25264 DKFZP434N126 protein 0.16 104037 AA372630 Hs. 100347 differentially expressed in hematopoieti 0.16 101461 M22430 Hs. 76422 phospholipase A2; group IIA (platelets; 0.16 116551 D20458 Hs. 229071 EST 0.16 133889 AA099391 Hs. 211582 myosin; light polypeptide kinase 0.16 103653 Z70295 Hs. 32966 guanylate cyclase activator 2B (uroguany 0.16 101070 L02785 Hs. 1650 down-regulated in adenoma 0.17 131501 AA121127 Hs. 181307 H3 histone; family 3A 0.17 133515 X98311 Hs. 74466 carcinoembryonic antigen-related cell ad 0.17 108604 AA099820 Hs. 49696 ESTs 0.17 132982 L02326 Hs. 198118 immunoglobulin lambda-like polypeptide 2 0.17 131676 C20785 Hs. 30514 ESTs 0.17 134675 AA250745 Hs. 87773 protein kinase; cAMP-dependent; catalyti 0.17 133441 M82962 Hs. 179704 meprin A; alpha (PABA peptide hydrolase) 0.18 130455 X17059 Hs. 155956 N-acetyltransferase 1 (arylamine N-acety 0.18 131734 D62965 Hs. 31297 ESTs 0.18 100749 HG3521-HT3715 Ras-Related Protein Rap1b 0.18 116724 F13665 Hs. 65641 ESTs 0.18 129265 X68277 Hs. 171695 dual specificity phosphatase 1 0.18 102347 U37518 Hs. 83429 tumor necrosis factor (ligand) superfami 0.18 114542 AA055768 Hs. 122576 ESTs 0.18 123900 AA621223 Hs. 112953 EST 0.19 121780 AA422086 Hs. 124660 ESTs 0.19 115662 AA405715 Hs. 64179 hypothetical protein 0.19 113803 W42789 Hs. 31446 ESTs 0.19 105493 AA256268 Hs. 10283 ESTs 0.19 113195 T57112 yc20g11.s1 Stratagene lung(#937210) Hom 0.19 129462 D84239 Hs. 111732 IgG Fc binding protein 0.19 133664 X86693 Hs. 75445 hevin 0.2 126180 R18070 Hs. 3712 ubiquinol-cytochrome c reductase; Rieske 0.2 100687 HG3115-HT3291 Golli-Mbp (Gb: L18862) 0.2 130064 T67053 Hs. 181125 immunoglobulin lambda gene cluster 0.2 101367 M12963 Hs. 73843 alcohol dehydrogenase 1 (class I); alpha 0.2 132254 L20826 Hs. 430 plastin 1 (I isoform) 0.2 105646 AA282147 Hs. 5888 ESTs 0.2 132883 AA047151 Hs. 5897 Homo sapiens mRNA; cDNA DKFZp586P1622 (f 0.21 132618 AA253330 Hs. 5344 adaptor-related protein complex 1; gamma 0.21 108931 AA147186 Hs. 250746 ESTs 0.22 131421 X64177 Hs. 2667 metallothionein 1H 0.22 107295 T34527 Hs. 80120 UDP-N-acetyl-alpha-D-galactosamine:polyp 0.22 103576 Z26317 Hs. 2631 desmoglein 2 0.22 105173 AA182030 Hs. 8364 ESTs 0.22 134843 H60595 Hs. 90061 progesterone binding protein 0.22 102009 U02680 Hs. 82643 protein tyrosine kinase 9 0.23 123997 D51171 Hs. 78902 voltage-dependent anion channel 2 0.23 106609 AA458652 Hs. 32181 ESTs 0.23 101300 L40391 Hs. 6445 Homo sapiens (clone s153) mRNA fragment 0.23 129717 AA481670 Hs. 12150 ESTs; Weakly similar to retinal short-ch 0.23 108565 AA085342 Hs. 1526 ATPase; Ca++ transporting; cardiac muscl 0.23 121314 AA402799 Hs. 182538 ESTs 0.23 124803 R45480 Hs. 164866 cyclin K 0.23 130208 AA620556 Hs. 15250 peroxisomal D3;D2-enoyl-CoA isomerase 0.23 132888 AA490775 Hs. 5920 UDP-N-acetylglucosamine-2-epimerase/N-ac 0.23 132720 Z69881 Hs. 5541 ATPase; Ca++ transporting; ubiquitous 0.23 102239 U26726 Hs. 1376 hydroxysteroid (11-beta) dehydrogenase 2 0.23 115764 AA421562 Hs. 91011 anterior gradient 2 (Xenepus laevis) hom 0.24 130558 H96654 Hs. 15984 ESTs; Weakly similar to gene pp21 protei 0.24 122666 AA455052 Hs. 99387 ESTs 0.24 134495 D63477 Hs. 84087 KIAA0143 protein 0.24 124017 F02202 Hs. 100960 ESTs 0.24 106925 AA491261 Hs. 37558 Homo sapiens clone 23923 mRNA sequence 0.24 115187 AA261805 Hs. 44021 ESTs 0.24 105309 AA233790 Hs. 4104 ESTs; Weakly similar to cDNA EST yk386g7 0.24 124457 N50114 Hs. 128704 ESTs 0.24 130616 AA233763 Hs. 16726 Homo sapiens mRNA; cDNA DKFZp564A132 (fr 0.25 105795 AA369245 Hs. 17448 ESTs; Weakly similar to !!!! ALU SUBFAMI 0.25 134579 N23222 Hs. 85963 CD36 antigen (collagen type I receptor; 0.25

[0339] TABLE 13 H chip - Met vs Normal query - up in Mets Pkey Ex Accn UniG_ID Complete_Title Ratio Met/Normal 102193 U20758 Hs. 313 secreted phosphoprotein 1 (osteopontin; 8.457 111307 N73988 Hs. 37477 ESTs; Weakly similar to CGI-141 protein 6.05 103119 X63629 Hs. 2877 cadherin 3; P-cadherin (placental) 5.207 131564 AA491456 Hs. 28792 ESTs 5.136 119729 W69747 Hs. 94806 KIAA1062 protein 4.667 124059 F13673 Hs. 99769 ESTs 4.398 123987 C21171 Hs. 95497 ESTs; Weakly similar to GLUCOSE TRANSPOR 4.292 128817 N47524 Hs. 28491 spermidine/spermine N1-acetyltransferase 3.964 133770 M69197 Hs. 242279 haptoglobin-related protein 3.823 130412 AA406554 Hs. 241572 golgi autoantigen; golgin subfamily a; 5 3.719 104755 AA024482 Hs. 9029 DKFZP434G032 protein 3.702 132676 AA283035 Hs. 54813 ESTs 3.645 134453 X70683 Hs. 83484 SRY (sex determining region Y)-box 4 3.581 124690 R05818 Hs. 173830 ESTs 3.446 106949 AA496805 Hs. 177425 KIAA0964 protein 3.42 130724 AA370091 Hs. 179680 ESTs 3.402 128992 R49693 Hs. 107708 ESTs 3.32 133421 AA436560 Hs. 7327 claudin 1 3.255 103047 X55990 Hs. 73839 ribonuclease; RNase A family; 3 (eosinop 3.229 102990 X51441 Hs. 181062 serum amyloid A1 3.149 115429 AA284139 Hs. 89295 EST 3.114 129158 J05257 Hs. 109 dipeptidase 1 (renal) 3.019 123533 AA608751 Hs. 244904 ESTs; Weakly similar to !!!! ALU SUBFAMI 3.011

[0340] TABLE 14 H chip - Met vs Normal query - down in Mets PkeyY Ex Accn UniG_ID Complete_Title Ratio Met/Normal 103466 Y00339 Hs. 155097 carbonic anhydrase II 0.012 104258 AF007216 Hs. 5462 solute carrier family 4; sodium bicarbon 0.025 108999 AA156064 Hs. 72115 ESTs 0.034 101046 K01160 Accession not listed in Genbank 0.041 133565 H57056 Hs. 204831 ESTs 0.042 101346 L76465 Hs. 77348 hydroxyprostaglandin dehydrogenase 15-(N 0.043 102095 U11313 Hs. 75760 sterol carrier protein 2 0.054 111855 R37362 Hs. 21351 ESTs 0.055 130320 U19495 Hs. 237356 stromal cell-derived factor 1 0.058 123137 AA487468 Hs. 100686 ESTs; Weakly similar to secreted cement 0.06 107222 D51235 Hs. 82689 tumor rejection antigen (gp96) 1 0.06 102638 U67319 Hs. 9216 caspase 7; apoptosis-related cysteine pr 0.063 128906 AA487557 Hs. 10706 ESTs 0.065 129105 AA224351 Hs. 108681 ESTs 0.069 110837 N30796 Hs. 17424 ESTs; Weakly similar to semaphorin F [H. 0.069 100116 D00654 Hs. 77443 actin; gamma 2; smooth muscle; enteric 0.071 116786 H25836 Hs. 83429 tumor necrosis factor (ligand) superfami 0.074 130867 J04093 Hs. 2056 UDP glycosyltransferase 1 0.075 132836 F09557 Hs. 57929 slit (Drosophila) homolog 3 0.076 131861 D11925 Hs. 184245 KIAA0929 protein Msx2 interacting nuclea 0.081 106674 AA461303 Hs. 7946 DKFZP586D1519 protein 0.084 109272 AA195718 Hs. 86030 ESTs 0.088 132711 N73702 Hs. 238927 ESTs 0.091 106569 AA455983 Hs. 117816 sorcin 0.092 104636 AA004415 Hs. 106106 ESTs 0.093 118823 N79237 Hs. 50813 ESTs; Weakly similar to long chain fatty 0.094 134534 X73501 Hs. 84905 H. Sapiens mRNA for cytokeratin 20 0.095 119479 W32094 Hs. 55501 ESTs 0.096 113778 W15263 Hs. 5422 ESTs 0.098 128482 U83908 Hs. 100407 programmed cell death 4 0.102 124653 N92884 Hs. 109641 ESTs 0.106 133407 AA093348 Hs. 7306 secreted frizzled-related protein 1 0.108 135237 AA454930 Hs. 9691 ESTs 0.109 116250 AA480975 Hs. 44829 ESTs 0.111 132617 AA171913 Hs. 5338 carbonic anhydrase XII 0.112 131273 AA421139 Hs. 173542 ESTs 0.113 116710 F10577 Hs. 70312 ESTs 0.114 131791 S71043 Hs. 32225 immunoglobulin alpha 1 0.114 112483 R66534 Hs. 28403 ESTs 0.115 132017 W67251 Hs. 37331 Homo sapiens vav 3 oncogene (VAV3) mRNA 0.116 124308 H93575 Hs. 227146 Homo sapiens mRNA; cDNA DKFZp564J142 (fr 0.117 114846 AA234929 Hs. 44343 ESTs 0.119 116551 D20458 Hs. 229071 EST 0.12 105299 AA233511 Hs. 194720 ATP-binding cassette; sub-family G (WHIT 0.122 130366 L11708 Hs. 155109 hydroxysteroid (17-beta) dehydrogenase 2 0.122 133806 M12759 Hs. 76325 Human Ig J chain gene 0.122 104776 AA026349 Hs. 31412 ESTs 0.125 129565 X77777 Hs. 198726 vasoactive intestinal peptide receptor 1 0.125 131272 AA423884 Hs. 139033 paternally expressed gene 3 0.127 105774 AA348014 Hs. 23412 ESTs 0.128 134604 M22995 Hs. 865 RAP1A; member of RAS oncogene family 0.128 134711 X04011 Hs. 88974 cytochrome b-245; beta polypeptide (chro 0.128 129113 AA147646 Hs. 108740 DKFZP586A0522 protein 0.133 123995 D51119 Hs. 100090 tetraspan 3 0.133 129168 T90621 Hs. 109052 chromosome 14 open reading frame 2 0.133 123891 AA621103 Hs. 99216 ESTs; Moderately similar to !!!! ALU SUB 0.135 132694 M60830 Hs. 5509 ecotropic viral integration site 2B 0.135 135342 W60097 Hs. 99120 DEAD/H (Asp-Glu-Ala-Asp/His) box polypep 0.135 131510 AA207114 Hs. 27842 ESTs; Weakly similar to similar to 1-acy 0.137 133652 AA287383 Hs. 7540 ESTs 0.137 134749 L10955 Hs. 89485 carbonic anhydrase IV 0.139 106586 AA456598 Hs. 256269 ESTs 0.139 106893 AA489636 Hs. 25253 ESTs 0.139 101070 L02785 Hs. 1650 down-regulated in adenoma 0.14 114293 Z40718 Hs. 20196 adenylate cyclase 9 0.14 113966 W86600 Hs. 9842 ESTs 0.141 101185 L19872 Hs. 170087 aryl hydrocarbon receptor 0.145 131492 AA393876 Hs. 1255 nuclear receptor subfamily 2; group F; m 0.145 133889 AA099391 Hs. 211582 myosin; light polypeptide kinase 0.145 120914 AA377254 Hs. 97107 EST 0.147 118771 N74690 Hs. 50547 ESTs 0.149 105496 AA256323 Hs. 25264 DKFZP434N126 protein 0.151 131011 R41771 Hs. 22146 ESTs 0.153 106210 AA428239 Hs. 10338 ESTs 0.154 114069 Z38161 Hs. 197335 plasma glutamate carboxypeptidase 0.154 133011 AA042990 Hs. 171921 sema domain; immunoglobulin domain (Ig); 0.154 115967 AA446887 Hs. 42911 ESTs 0.154 102571 U60115 Homo sapiens skeletal muscle LIM-protein 0.155 100687 HG3115-HT3291 Golli-Mbp (Gb: L18862) 0.155 132903 AA235404 Hs. 5985 Homo sapiens clone 25186 mRNA sequence 0.155 125832 AA628600 Hs. 117587 ESTs 0.155 130064 T67053 Hs. 181125 immunoglobulin lambda gene cluster 0.157 123264 AA491003 Hs. 99824 BCE-1 protein 0.159 130919 AA291710 Hs. 21276 collagen; type IV; alpha 3 (Goodpasture 0.159 103542 Z11793 Hs. 3314 selenoprotein P; plasma; 1 0.161 101478 M23379 Hs. 758 RAS p21 protein activator (GTPase activa 0.162 108921 AA142913 Hs. 71721 ESTs 0.164 100642 HG2743-HT3926 Caldesmon 1, Alt. Splice 6, Non-Muscle 0.167 132109 AA599801 Hs. 40098 ESTs 0.167 115719 AA416997 Hs. 59622 ESTs 0.169 128915 C02386 Hs. 107139 ESTs 0.171 117634 N36421 Hs. 107854 ESTs; Weakly similar to SODIUM-AND CHLO 0.172 129462 D84239 Hs. 111732 IgG Fc binding protein 0.174 131328 V01512 Hs. 25647 v-fos FBJ murine osteosarcoma viral onco 0.176 130343 AA490262 Hs. 15485 ESTs; Weakly similar to APICAL-LIKE PROT 0.177 115764 AA421562 Hs. 91011 anterior gradient 2 (Xenepus laevis) hom 0.177 122261 AA436830 Hs. 98902 ESTs 0.179 106605 AA457718 Hs. 21103 Homo sapiens mRNA; cDNA DKFZp564B076 (fr 0.179 109991 H09813 Hs. 12896 KIAA1034 protein 0.181 101300 L40391 Hs. 6445 Homo sapiens (clone s153) mRNA fragment 0.181 123080 AA485303 Hs. 205126 polymeric immunoglobulin receptor 0.182 130016 AA055811 Hs. 143131 transmembrane glycoprotein 0.186 122666 AA455052 Hs. 99387 ESTs 0.188 105453 AA252893 Hs. 9001 ESTs 0.189 108980 AA151676 Hs. 33455 peptidyl arginine deiminase; type II 0.19 100248 D31888 Hs. 78398 KIAA0071 protein 0.192 130036 AA195260 Hs. 206738 ESTs; Moderately similar to !!!! ALU SUB 0.192 110882 N36001 Hs. 17348 ESTs; Weakly similar to !!!! ALU SUBFAMI 0.193 131676 C20785 Hs. 30514 ESTs 0.195 111029 N54792 Hs. 24697 cytidine monophosphate-N-acetylneuramini 0.196 131257 AA256042 Hs. 24908 ESTs 0.196 133348 T23517 Hs. 7149 ESTs 0.196 133784 AA214305 Hs. 76173 ESTs 0.196 113863 W68388 Hs. 21288 ESTs; Weakly similar to KIAA0704 protein 0.197 103158 X67235 Hs. 118651 hematopoietically expressed homeobox 0.198 102347 U37518 Hs. 83429 tumor necrosis factor (ligand) superfami 0.2 111351 N90223 Hs. 23392 ESTs 0.2 123495 AA599850 Hs. 106747 ESTs; Weakly similar to similar to BPTV 0.2 123802 AA620448 Hs. 61408 Homo sapiens clone 24760 mRNA sequence 0.2 129243 H88033 Hs. 109727 KIAA0733 protein 0.2 130219 R77539 Hs. 15285 ESTs 0.2 131171 H04644 Hs. 167619 ESTs; Weakly similar to !!!! ALU SUBFAMI 0.2 133746 U44378 Hs. 75862 MAD (mothers against decapentaplegic; Dr 0.2 116459 AA621399 Hs. 64193 ESTs 0.201 109613 F03031 Hs. 27519 ESTs 0.202 133435 T23983 Hs. 7365 ESTs 0.202 103002 X52001 Hs. 1408 endothelin 3 0.204 125153 W38294 Accession not listed in Genbank 0.204 131919 AA121266 Hs. 34641 ESTs 0.204 100749 HG3521-HT3715 Ras-Related Protein Rap1b 0.205 105085 AA147537 Hs. 4811 ESTs 0.208 124571 N67470 Hs. 173074 DKFZP564O1863 protein 0.21 129519 AA298786 Hs. 112242 ESTs 0.21 116724 F13665 Hs. 65641 ESTs 0.21 132932 T15482 Hs. 6093 ESTs 0.21 113803 W42789 Hs. 31446 ESTs 0.211 110792 N24899 Hs. 6630 ESTs 0.212 105178 AA187490 Hs. 21941 ESTs 0.212 107295 T34527 Hs. 80120 UDP-N-acetyl-alpha-D-galactosamine: polyp 0.212 115262 AA279112 Hs. 88594 ESTs 0.213 115839 AA429038 Hs. 40541 ESTs 0.213 103211 X73079 Hs. 205126 polymeric immunoglobulin receptor 0.214 108604 AA099820 Hs. 49696 ESTs 0.215 105173 AA182030 Hs. 8364 ESTs 0.217 108539 AA084677 Hs. 54558 ESTs; Weakly similar to protein B [H.sap 0.217 109984 H09594 Hs. 10299 ESTs 0.217 133536 Y00264 Hs. 177486 amyloid beta (A4) precursor protein (pro 0.217 129965 T71333 Hs. 13854 ESTs 0.219 114542 AA055768 Hs. 122576 ESTs 0.219 132982 L02326 Hs. 198118 immunoglobulin lambda-like polypeptide 2 0.22 101809 M86849 Homo sapiens connexin 26 (GJB2) mRNA, co 0.222 105795 AA369245 Hs. 17448 ESTs; Weakly similar to !!!! ALU SUBFAMI 0.222 132119 H99211 Hs. 40334 ESTs 0.222 132733 R25385 Hs. 123654 KIAA0824 protein 0.222 109415 AA227219 Hs. 110826 trinucleotide repeat containing 9 0.222 113083 T40530 Hs. 8241 ESTs; Weakly similar to heat shock prote 0.223 107053 AA600147 Hs. 5741 ESTs; Weakly similar to NADH-cytochrome 0.224 103653 Z70295 Hs. 32966 guanylate cyclase activator 2B (uroguany 0.225 104613 AA001049 Hs. 24713 Homo sapiens mRNA; cDNA DKFZp586G0123 (f 0.225 126180 R18070 Hs. 3712 ubiquinol-cytochrome c reductase; Rieske 0.227 132015 D11900 Hs. 3731 ESTs 0.227 130616 AA233763 Hs. 16726 Homo sapiens mRNA; cDNA DKFZp564A132 (fr 0.227 132883 AA047151 Hs. 5897 Homo sapiens mRNA; cDNA DKFZp586P1622 (f 0.23 123169 AA488892 Hs. 104472 ESTs; Weakly similar to Gag-Pol polyprot 0.233 115187 AA261805 Hs. 44021 ESTs 0.234 116787 H28581 Hs. 15641 ESTs 0.234 113195 T57112 yc20g11.s1 Stratagene lung (#937210) Hom 0.235 130707 W45457 Hs. 203559 ESTs 0.235 124803 R45480 Hs. 164866 cyclin K 0.235 116844 H64938 Hs. 38331 ESTs 0.235 102759 U81607 Hs. 788 A kinase (PRKA) anchor protein (gravin) 0.238 130584 AA009839 Hs. 180841 tumor necrosis factor receptor superfami 0.238 133240 D31161 Hs. 68613 ESTs 0.238 132952 AA425154 Hs. 61426 ESTs 0.239 132720 Z69881 Hs. 5541 ATPase; Ca++ transporting; ubiquitous 0.24 131734 D62965 Hs. 31297 ESTs 0.24 111890 R38678 Hs. 12365 ESTs 0.241 102325 U35139 Hs. 50130 necdin (mouse) homolog 0.244 104968 AA084602 Hs. 29669 ESTs 0.244 105674 AA284755 Hs. 214742 CDW52 antigen (CAMPATH-1 antigen) 0.244 120519 AA258585 Hs. 129887 cadherin 19 (NOTE: redefinition of symbo 0.244 134675 AA250745 Hs. 87773 protein kinase; cAMP-dependent; catalyti 0.244 130642 M63438 Hs. 156110 Immunoglobulin kappa variable 1D-8 0.245 134418 R78190 Hs. 82933 ESTs; Weakly similar to cDNA EST EMBL: T0 0.245 115137 AA257976 Hs. 56156 ESTs 0.245 131713 X57809 Hs. 181125 immunoglobulin lambda gene cluster 0.246 108931 AA147186 Hs. 250746 ESTs 0.246 106609 AA458652 Hs. 32181 ESTs 0.248 115559 AA393810 Hs. 41067 ESTs 0.25 133985 L34657 Hs. 78146 platelet/endothelial cell adhesion molec 0.25 134088 D43636 Hs. 79025 KIAA0096 protein 0.25 134487 R38185 Hs. 83954 Homo sapiens unknown mRNA 0.25

[0341] TABLE 15 I chip - Met vs Normal query - up in Mets Pkey Ex_Accn UniG_ID Title Ratio Met/Normal 319379 T91443 Hs. 193963 ESTs 18.71 321920 N63915 EST cluster (not in UniGene) 11.9 314522 AI732331 Hs. 187750 ESTs; Moderately similar to !!!! ALU CLA 7.23 315720 AW291875 Hs. 163900 ESTs 6.06 308010 AI439190 Hs. 181165 eukaryotic translation elongation factor 5.76 313774 AW136836 Hs. 144583 ESTs 5.01 300734 AW205197 Hs. 240951 ESTs 3.98 337895 CH22_EM: AC005500.GENSCAN.56-2 3.98 312339 AA524394 EST cluster (not in UniGene) 3.66 331644 T99544 Hs. 173734 ESTs; Weakly similar to !!!! ALU CLASS B 3.53 324643 AI436356 Hs. 130729 ESTs 3.52 324302 AA543008 Hs. 136806 ESTs; Weakly similar to !!!! ALU SUBFAMI 3.41 314912 AI431345 Hs. 161784 ESTs 3.33 319403 T98413 EST cluster (not in UniGene) 3.32 308676 AI761036 EST singleton (not in UniGene) with exon 3.27 331858 AA421163 Hs. 163848 ESTs 3.22 315178 AW362945 Hs. 162459 ESTs 3.21 321354 AA078493 EST cluster (not in UniGene) 3.18 337898 CH22_EM: AC005500.GENSCAN.56-5 3.16 322682 AI110679 EST cluster (not in UniGene) 3.15 313197 AI738851 Hs. 222487 ESTs 3.1 308991 AI879831 EST singleton (not in UniGene) with exon 3.08 310016 AW449612 Hs. 152475 ESTs 3.05

[0342] TABLE 16 I chip - Met vs Normal query - down in Mets Pkey Ex_Accn UniG_ID title Ratio Met/Normal 303041 AF127035 EST cluster (not in UniGene) with exon h 0.02 302360 AJ010901 Hs. 198267 mucin 4; tracheobronchial 0.03 301948 AA344647 Hs. 116724 aldo-keto reductase family 1; member B11 0.03 336091 CH22_FGENES.689_3 0.04 333657 CH22_FGENES.241_2 0.04 333658 CH22_FGENES.241_4 0.04 333737 CH22_FGENES.261_1 0.05 333656 CH22_FGENES.240_4 0.05 302347 AF039400 Hs. 194659 chloride channel; calcium activated; fam 0.06 336084 CH22_FGENES.688_13 0.06 330385 AA449749 Hs. 31386 ESTs; Highly similar to secreted apoptos 0.06 304487 AA434241 EST singleton (not in UniGene) with exon 0.07 302292 AF067797 EST cluster (not in UniGene) with exon h 0.07 334030 CH22_FGENES.320_2 0.07 332859 CH22_FGENES.27_2 0.07 333654 CH22_FGENES.240_2 0.07 303270 AL120518 Hs. 105352 ESTs 0.08 320352 Y13323 Hs. 145296 disintegrin protease 0.08 333637 CH22_FGENES.229_2 0.08 324094 AA382603 EST cluster (not in UniGene) 0.08 320590 U67058 Hs. 168102 Human proteinase activated receptor-2 mR 0.08 330622 X63597 Hs. 2996 sucrase-isomaltase 0.08 331441 H75860 Hs. 39720 ESTs 0.08 308601 AI719930 EST singleton (not in UniGene) wilh exon 0.09 323770 AA722425 EST cluster (not in UniGene) 0.09 335188 CH22_FGENES.507_3 0.09 333730 CH22_FGENES.258_1 0.09 304480 AA430373 EST singleton (not in UniGene) with exon 0.09 336081 CH22_FGENES.688_10 0.1 332071 AA598594 Hs. 112475 ESTs 0.1 318538 N28625 Hs. 74034 caveolin 1; caveolae protein; 22 kD 0.1 311331 AI679622 Hs. 32225 immunoglobulin alpha 1 0.1 319668 NM_002731 EST cluster (not in UniGene) 0.11 332567 N23730 Hs. 25647 v-fos FBJ murine osteosarcoma viral onco 0.11 319395 AW062570 Hs. 13809 ESTs 0.11 315594 AI983437 Hs. 155145 ESTs 0.11 321539 N98619 Hs. 62461 ARP2 (actin-related protein 2; yeast) ho 0.12 333647 CH22_FGENES.235_2 0.12 333588 CH22_FGENES.206_2 0.12 321286 AI380940 EST cluster (not in UniGene) 0.12 320727 U96044 EST cluster (not in UniGene) 0.13 335687 CH22_FGENES.596_2 0.13 324611 AA743462 Hs. 165337 ESTs 0.14 335115 CH22_FGENES.496_2 0.14 324660 AA541644 Hs. 186044 ESTs 0.14 337951 CH22_EM: AC005500.GENSCAN.94-1 0.14 302332 AI833168 Hs. 184507 Homo sapiens Chromosome 16 BAC clone CIT 0.14 300921 AW293224 Hs. 232165 ESTs 0.14 333646 CH22_FGENES.234_2 0.14 335116 CH22_FGENES.496_3 0.14 320211 AL039402 Hs. 125783 DEME-6 protein 0.15 336092 CH22_FGENES.689_6 0.15 330673 D57823 Hs. 92962 Sec23 (S. cerevisiae) homolog A 0.16 303042 AF129532 EST cluster (not in UniGene) with exon h 0.16 337954 CH22_EM: AC005500.GENSCAN.96-3 0.16 336645 CH22_FGENES.26-1 0.16 335651 CH22_FGENES.590_2 0.16 314499 AL044570 Hs. 147975 ESTs 0.17 336124 CH22_FGENES.701_9 0.17 315199 AA877996 Hs. 125376 ESTs 0.17 324525 AW044647 Hs. 196284 ESTs 0.17 320825 NM_004751 EST cluster (not in UniGene) 0.18 302049 AA377072 Hs. 129792 Homo sapiens Chromosome 16 BAC clone CIT 0.18 336083 CH22_FGENES.688_12 0.18 333653 CH22_FGENES.239_2 0.18 323243 W44372 EST cluster (not in UniGene) 0.19 316610 AW087973 Hs. 126731 ESTs 0.19 315033 AI493046 Hs. 146133 ESTs 0.19 330551 U39840 Hs. 105440 hepatocyte nuclear factor 3; alpha 0.19 333642 CH22_FGENES.231_2 0.19 301281 AA843986 Hs. 190586 ESTs 0.2 333626 CH22_FGENES.224_2 0.21 303792 C75094 Hs. 199839 ESTs; Highly similar to NG22 [H. sapiens] 0.21 332325 T79428 Hs. 191264 ESTs 0.21 321223 AA431366 EST cluster (not in UniGene) 0.21 333635 CH22_FGENES.228_2 0.22 314645 AI808999 Hs. 207570 ESTs 0.22 322929 AI365585 Hs. 146246 ESTs 0.22 324718 AI557019 Hs. 116467 ESTs 0.22 335652 CH22_FGENES.590_3 0.22 307783 AI347274 EST singleton (not in UniGene) with exon 0.22 331344 AA357927 Hs. 70208 ESTs 0.22 336088 CH22_FGENES.688_17 0.23 320802 D83824 Hs. 185055 BENE protein 0.23 335692 CH22_FGENES.596_7 0.23 333593 CH22_FGENES.210_2 0.23 335667 CH22_FGENES.590_18 0.24 314853 AA729232 Hs. 153279 ESTs 0.24 320244 AA296922 Hs. 129778 gastrointestinal peptide 0.24 300601 AI762130 Hs. 165619 ESTs 0.24 305080 AA641485 EST singleton (not in UniGene) with exon 0.25 335189 CH22_FGENES.507_4 0.25

[0343] TABLE 17 B survivor vs Mets - Up in B survivor Pkey Ex Accn UniG_ID Complete Title Ratio BS/Met 101006 J04132 Hs. 97087 CD3Z antigen; zeta polypeptide (TiT3 com 7.28 114173 Z39050 Hs. 21963 ESTs 6.13 130284 X82206 Hs. 153961 ARP1 (actin-related protein 1; yeast) ho 5.77 100787 HG3872-HT4142 Immunoglobulin Gamma Heavy Chain, V(6)Djc Regions (Gb: U13200) 5.63 132461 AA405775 Hs. 49005 hypothetical protein 5.62 133806 M12759 Hs. 76325 Human Ig J chain gene 5.46 133747 D86972 Hs. 75863 KIAA0218 gene product 5.45 123328 AA496968 Hs. 105403 EST 5.28 132671 X76302 Hs. 54649 putative nucleic acid binding protein RY 5.25 132018 AA293194 Hs. 3737 ESTs 5.22 100186 D17516 Hs. 4748 adenylate cyclase activating polypeptide 5.14 107155 AA621202 Hs. 7946 DKFZP586D1519 protein 5.1 103566 Z22555 Hs. 180616 CD36 antigen (collagen type I receptor; 5.06 113355 T79203 Hs. 14480 ESTs 4.99 129040 U38864 Hs. 108139 zinc finger protein 212 4.96 130214 H78003 Hs. 15266 ESTs 4.93 129550 AA480991 Hs. 113025 ESTs 4.92 129704 W81301 Hs. 12064 ubiquitin specific protease 22 4.91 116425 AA609574 Hs. 51483 ESTs 4.77 105166 AA179787 Hs. 30570 polyglutamine binding protein 1 4.65 118765 N74442 Hs. 183696 ESTs 4.6 108999 AA156064 Hs. 72115 ESTs 4.57 112756 R93908 Hs. 35258 ESTs 4.54 111655 R16884 Hs. 187462 ESTs 4.48 119392 T90672 Hs. 238859 ESTs 4.42 131957 AA609008 Hs. 183232 ESTs 4.41 129275 D82061 Hs. 109993 Ke6 gene; mouse; human homolog of 4.4 113634 T95085 Hs. 125182 ESTs 4.4 127187 AA297138 Hs. 207422 ESTs 4.32 101147 L13266 Hs. 105 glutamate receptor; ionotropic; N-methyl 4.3 134901 S78873 Hs. 90875 RAB interacting factor 4.26 100896 HG4593-HT4998 Sodium Channel 1 4.24 100687 HG3115-HT3291 Golli-Mbp (Gb: L18862) 4.21 129758 AA599552 Hs. 183770 Homo sapiens mRNA; cDNA DKFZp566P2346 (f 4.19 105440 AA252243 Hs. 22851 ESTs 4.16 131551 AA127867 Hs. 28608 ESTs 4.15 113761 T99373 Hs. 189786 ESTs 4.09 105897 AA401091 ESTs 4.07 129495 AA382529 Hs. 239676 ESTs 4.06 103436 X98206 H. sapiens mRNA for UV-B repressed sequen 4.03 104673 AA007633 Hs. 20010 ESTs 4.03 128886 L36720 Hs. 106880 bystin-like 4.02 100702 HG3236-HT3413 Neurofibromatosis 2 Tumor Suppressor (Gb: L27065) 3.99 123547 AA608820 Hs. 124085 KIAA0921 protein 3.98 134877 AA455241 Hs. 90527 ESTs 3.97 123650 AA609332 Hs. 180696 ESTs 3.94 106482 AA451672 Hs. 108824 ESTs; Weakly similar to cDNA EST yk415c1 3.94 101909 S69265 Homo sapiens mRNA for PLE21 protein; com 3.93 108390 AA075070 zm86b6.s1 Stratagene ovarian cancer (#93 3.93 LYMPHOCYTE ANTIGEN LY-6A.2/LY-6E.1 PREC 135403 U06643 Hs. 99923 lectin; galactoside-binding; soluble; 7 3.89 121038 AA398536 Hs. 97365 ESTs 3.88 128496 T83496 Hs. 100610 ESTs 3.86 108785 AA128946 ESTs 3.86 119838 W79499 Hs. 58580 ESTs 3.85 130109 L12060 Hs. 1497 retinoic acid receptor; gamma 3.84 134538 U79288 Hs. 85053 KIAA0513 gene product 3.83 110310 H38209 Hs. 32728 EST 3.81 110433 H49425 Hs. 32992 ESTs 3.78 111834 R36138 Hs. 152458 ESTs 3.76 130903 N27086 Hs. 21068 ESTs 3.74 105142 AA164851 Hs. 15380 ESTs; Weakly similar to HERV-E envelope 3.73 130248 U84569 Hs. 153452 chromosome 21 open reading frame 2 3.73 130645 AA020942 Hs. 17200 STAM-like protein containing SH3 and ITA 3.73 123378 AA521043 Hs. 185832 ESTs 3.73 103985 AA313880 EST185737 Colon carcinoma (HCC) cell in 3.73 112397 R60822 Hs. 26805 EST 3.72 100980 J03069 Hs. 72931 v-myc avian myelocytomatosis viral oncog 3.72 102609 U64863 Hs. 158297 programmed cell death 1 3.7 108974 AA151402 Hs. 46531 ESTs 3.7 130192 Y12661 Hs. 171014 VGF nerve growth factor inducible 3.69 131318 X51699 Hs. 2558 bone gamma-carboxyglutamate (gla) protei 3.68 113759 T99364 Hs. 16074 Homo sapiens mRNA; cDNA DKFZp564|153 (fr 3.66 133712 L19267 Hs. 198836 dystrophia myotonica-containing WD repea 3.65 134229 R15108 Hs. 8037 ESTs 3.65 134241 AA300265 Hs. 80540 KIAA0195 gene product 3.65 124699 R06413 Hs. 112278 arrestin; beta 1 3.62 107343 U03115 Hs. 103945 Human V beta T-cell receptor (TCRBV) gen 3.62 128511 AA425636 Hs. 10082 potassium intermediate/small conductance 3.62 105466 AA253412 Hs. 21489 ESTs 3.61 131377 R41389 Hs. 26159 ESTs 3.6 119135 R49548 Hs. 169681 death effector domain-containing 3.6 132982 L02326 Hs. 198118 immunoglobulin lambda-like polypeptide 2 3.59 128514 H84261 Hs. 100843 ESTs; Weakly similar to similar to GTP-b 3.56 102396 U41804 Hs. 54411 putative T1/ST2 receptor binding protein 3.55 134945 R50247 Hs. 91600 ESTs 3.55 134913 X60483 Hs. 91031 H4 histone family; member D 3.54 102053 U07664 Hs. 37035 homeo box HB9 3.52 121569 AA412686 Hs. 97955 ESTs 3.52 132560 AA005315 Hs. 204524 ESTs; Weakly similar to KIAA0747 protein 3.51 118456 N66580 Hs. 161496 EST; Weakly similarto HC1 ORF [M.muscul 3.51 111518 R08160 Hs. 222529 ESTs; Weakly similar to !!!! ALU SUBFAMI 3.51 116795 H38858 Hs. 251783 EST 3.5 130377 AA378316 Hs. 155182 KIAA1036 protein 3.5 121774 AA421756 Hs. 98361 ESTs 3.49 123413 AA521448 Hs. 103845 ESTs 3.49 133798 AA444115 Hs. 76277 ESTs; Weakly similar to salivary proline 3.49 135183 X93996 Hs. 239663 myeloid/lymphoid or mixed-lineage leukem 3.48 132479 AA477715 Hs. 4953 golgi autoantigen; golgin subfamily a; 3 3.47 117191 H99394 Hs. 40339 EST 3.47 130942 X87852 Hs. 21432 H. sapiens mRNA for SEX gene 3.46 130700 D55696 Hs. 18069 protease; cysteine; 1 (legumain) 3.43 131301 T17386 Hs. 164501 ESTs 3.43 100818 HG4018-HT4288 Opioid-Binding Cell Adhesion Molecule 3.43 103393 X94612 Hs. 41749 protein kinase; cGMP-dependent type II 3.43 131337 AA228116 Hs. 170204 KIAA0551 protein 3.42 133403 X68688 Hs. 72991 zinc finger protein 33b (KOX 31) 3.42 124728 R16231 Hs. 106620 Homo sapiens clone 23950 mRNA sequence 3.41 123168 AA488881 Hs. 105218 EST 3.39 123324 AA496932 Hs. 105399 KIAA0809 protein 3.38 106947 AA496685 Hs. 37936 suppressor of variegation 3-9 (Drosophil 3.38 116717 F11065 Hs. 79363 ESTs 3.36 102794 U88629 Hs. 173334 ELL-RELATED RNA POLYMERASE II; ELONGATIO 3.34 117503 N31963 Hs. 44286 ESTs 3.33 112220 R50295 Hs. 25703 ESTs 3.33 106340 AA441792 Hs. 22857 chord domain-containing protein 1 3.33 106308 AA436186 Hs. 30662 ESTs 3.32 130894 D16105 Hs. 210 leukocyte tyrosine kinase 3.31 120039 W92548 Hs. 94985 ESTs 3.31 131428 U17838 Hs. 26719 PR domain containing 2; with ZNF domain 3.3 113285 T66830 Hs. 182712 ESTs 3.3 109458 AA232648 Hs. 87068 ESTs 3.29 132134 AA242904 Hs. 40637 proline-rich Gla (G-carboxyglutamic acid 3.29 118964 N93330 Hs. 54937 Homo sapiens clone 24722 unknown mRNA; p 3.29 127621 AI218205 Hs. 116204 ESTs 3.29 135149 U40002 Hs. 95351 lipase; hormone-sensitive 3.28 114371 Z41835 Hs. 27810 ESTs 3.28 130043 AA055404 Hs. 193953 ESTs; Weakly similar to !!!! ALU SUBFAMI 3.27 121347 AA405181 Hs. 97972 ESTs 3.25 105754 AA302657 Hs. 192028 ESTs 3.25 121327 AA404286 Hs. 173125 peptidylprolyl isomerase F (cyclophilin 3.25 111204 N68295 Hs. 37982 ESTs 3.25 120949 AA397830 Hs. 98347 ESTs; Weakly similar to GLIOMA PATHOGENE 3.25 130024 U15197 Hs. 241560 Human histo-blood group ABO protein mRNA 3.24 125005 T61449 Hs. 193727 ESTs 3.24 121067 AA398662 Hs. 97302 ESTs 3.24 120996 AA398281 Hs. 143684 ESTs 3.23 117101 H94043 Hs. 24341 DKFZP586|1419 protein 3.23 130708 U40490 Hs. 18136 nicotinamide nucleotide transhydrogenase 3.23 130270 L40399 Hs. 153820 hypothetical protein 3.22 131605 AA256220 Hs. 29383 ESTs 3.22 100854 HG4194-HT4464 Sodium/Hydrogen Exchanger 5 3.22 123026 AA481072 Hs. 99743 ESTs 3.21 108328 AA070204 zm68b3.s1 Stratagene neuroepithelium (#9 3.2 104259 AF007833 Hs. 159265 Homo sapiens kruppel-related zinc finger 3.2 133711 J04130 Hs. 75703 small inducible cytokine A4 (homologous 3.2 112261 R52145 Hs. 25894 ESTs; Highly similar to hypothetical pro 3.19 119529 W38053 Accession not listed in Genbank 3.19 122386 AA446221 Hs. 6092 F-box protein containing leucine-rich re 3.19 109157 AA179161 Hs. 73562 ESTs 3.19 119903 W85707 Hs. 75936 erythrocyte membrane protein band 4.9 (d 3.18 127452 AA491317 aa65c01.r1 NCI_CGAP_GCB1 Homo sapiens cD 3.18 124229 H62793 Hs. 221892 ESTs 3.18 129221 AA417126 Hs. 109571 translocase of inner mitochondrial membr 3.17 133185 AA481404 Hs. 6686 ESTs 3.16 121479 AA411911 Hs. 98110 ESTs 3.16 133872 T79868 Hs. 180903 hypothetical protein 3.16 132504 U12897 Hs. 5022 imprinted in Prader-Willi syndrome 3.16 103089 X60382 Hs. 179729 collagen; type X; alpha 1 (Schmid metaph 3.15 129654 AA019943 Hs. 118463 H. sapiens mRNA for unknown liver orphan 3.15 117295 N22360 Hs. 43153 ESTs 3.15 107349 U48224 Hs. 158321 beaded filament structural protein 2; ph 3.14 103451 X99459 Hs. 154782 adaptor-related protein complex 3; sigma 3.14 114854 AA235056 Hs. 120244 ESTs 3.14 121044 AA398551 Hs. 97374 ESTs 3.13 128582 U22963 Hs. 101840 major histocompatibility complex; class 3.13 112598 R78565 Hs. 138395 EST 3.13 113170 T54342 Hs. 222506 ESTs 3.13 111714 R23146 Hs. 23466 ESTs 3.13 111809 R33616 Hs. 24688 EST 3.12 115249 AA278961 Hs. 71124 ESTs 3.11 103228 X75546 Hs. 230 fibromodulin 3.11 129944 L00389 Hs. 1361 cytochrome P450; subfamily I (aromatic c 3.11 107927 AA028915 Hs. 237709 EST 3.11 130297 H94949 Hs. 171955 trophinin-assisting protein (tastin) 3.1 125742 H81181 Hs. 183654 ESTs; Weakly similar to unknown [S.cerev 3.1 134802 L35548 Hs. 89709 glutamate-cysteine ligase (gamma-glutamy 3.1 112560 R72293 Hs. 6179 Homo sapiens mRNA; cDNA DKFZp586K2322 (f 3.1 129266 AA343881 Hs. 209061 sudD (suppressor of bimD6; Aspergillus n 3.09 126982 AA211419 small inducible cytokine A5 (RANTES) 3.09 131594 H29723 Hs. 29261 ESTs; Weakly similar to serine protease 3.08 134910 AA431320 Hs. 9100 ESTs 3.08 103505 Y09912 Hs. 33102 transcription factor AP-2 beta (activati 3.08 110525 H57330 Hs. 37430 EST 3.07 123276 AA491270 Hs. 187946 ESTs 3.06 130519 H91819 Hs. 10669 ESTs; Moderately similar to KIAA0400 [H. 3.06 126621 AA192638 zq01h08.r1 Stratagene muscle 937209 Homo 3.05 134327 AF006041 Hs. 178743 death-associated protein 6 3.04 103513 Y10209 H. sapiens mRNA for CD3L protein 3.04 131243 R16667 Hs. 24752 spectrin SH3 domain binding protein 1 3.04 115187 AA261805 Hs. 44021 ESTs 3.04 107543 Z43703 Hs. 4552 Homo sapiens HRIHFB2157 mRNA; partial cd 3.04 134051 S67070 Hs. 78846 heat shock 27 kD protein 2 3.04 113461 T86737 Hs. 193536 ESTs 3.03 130490 X57522 Hs. 158164 ATP-binding cassette; sub-family B (MDR/ 3.03 128843 AA234141 Hs. 203004 katanin p80 (WD40-containing) subunit B 3.03 100941 HG862-HT862 Transition Protein 2 3.03 122268 AA436855 Hs. 178202 ESTs 3.02 107425 W26719 Hs. 30204 ESTs 3.02 130930 U19261 TNF receptor-associated factor 1 3.02 132958 W90398 Hs. 6147 KIAA1075 protein 3.02 100973 J02888 Hs. 73956 NAD(P)H menadione oxidoreductase 2; diox 3.01 104924 AA058532 Hs. 28774 ESTs 3.01 129998 Y10055 Hs. 162808 phosphoinositide-3-kinase; catalytic; de 3.01 130023 X13401 Hs. 239600 calmodulin-like 3 3.01 129536 M33493 Hs. 184504 tryptase; alpha 3 112015 R42836 Hs. 23198 ESTs 3 103036 X54925 Hs. 83169 matrix metalloproteinase 1 (interstitial 2.99 100756 HG3565-HT3768 Zinc Finger Protein (Gb: M88357) 2.99 103425 X97301 H. sapiens mRNA for Ptg-11 protein 2.99 118291 N63076 Hs. 138745 EST 2.98 125877 H15229 ym30g04.r1 Soares infant brain 1NIB Homo 2.98 repetitive element;, mRNA sequence. 101371 M13232 Hs. 36989 coagulation factor VII (serum prothrombi 2.98 102958 X15675 Hs. 93174 Human endogenous retrovirus pHE.1 (ERV9) 2.97 121183 AA400138 Hs. 97703 ESTs 2.97 119241 T12559 Hs. 221382 ESTs 2.96 115067 AA253458 Hs. 91299 postmeiotic segregation increased 2-like 2.96 126196 AA084394 zn05g10.s1 Stratagene hNT neuron (#93723 2.96 111642 R16153 Hs. 128740 ESTs; Highly similar to DNb-5 [H. sapiens 2.95 100898 HG4638-HT5050 Spliceosomal Protein Sap 49 2.95 129370 AA287879 Hs. 110796 ESTs; Moderately similar to GTP-binding 2.94 128915 C02386 Hs. 107139 ESTs 2.94 101868 M96233 Hs. 82891 glutathione S-transferase M4 2.94 124394 N29724 gamma2-adaptin 2.93 103559 Z19585 Hs. 75774 thrombospondin 4 2.93 107882 AA025630 Hs. 17801 ESTs; Moderately similar to serine/proli 2.93 134919 T99639 Hs. 91142 KH-type splicing regulatory protein (FUS 2.92 110293 H30258 Hs. 37165 collagen; type IX; alpha 2 2.92 132433 AA082546 Hs. 48516 ESTs 2.92 127347 AA428350 ESTs 2.92 121976 AA429807 Hs. 98632 ESTs 2.91 133025 AA135492 Hs. 6318 ESTs; Highly similar to peroxisomal shor 2.91 133413 S72043 Hs. 73133 metallothionein 3 (growth inhibitory fac 2.91 111694 R22035 Hs. 23331 ESTs 2.91 128369 F12681 Hs. 205300 ESTs 2.9 102464 U49260 Hs. 3828 mevalonate (diphospho) decarboxylase 2.9 135358 C21431 Hs. 99486 ESTs; Weakly similar to aralar1 [H.sapie 2.9 108661 AA113287 Hs. 65905 ESTs; Weakly similar to PTB-ASSOCIATED S 2.9 102185 U20230 Human guanyl cyclase C gene, partial cds 2.89 122071 AA431787 Hs. 98762 EST 2.89 102040 U06088 Hs. 159479 galactosamine (N-acetyl)-6-sulfate sulfa 2.89 115689 AA410645 Hs. 199014 ESTs 2.88 135110 T15817 Hs. 193788 nitric oxide synthase 2A (inducible; hep 2.88 118729 N73717 Hs. 161526 EST 2.88 129518 AA369807 Hs. 112238 ESTs 2.88 125788 R74309 Hs. 44499 small EDRK-rich factor 2 2.87 128650 U57971 Hs. 103124 ATPase; Ca++ transporting; plasma membra 2.87 125936 H30751 Hs. 182859 lifeguard 2.87 100779 HG3731-HT4001 Immunoglobulin Heavy Chain, Vdjrc Regions (Gb: L23566) 2.87 104451 M13299 Hs. 102119 blue cone pigment 2.86 133539 M21574 Hs. 74615 platelet-derived growth factor receptor; 2.86 119506 W37833 Hs. 55563 ESTs 2.86 126568 AA190515 zp85d12.r1 Stratagene HeLa cell s3 93721 2.86 134184 X53742 Hs. 79732 fibulin 1 2.86 127633 AI339609 Hs. 152733 potassium voltage-gated channel; Isk-rel 2.86 128716 AA045978 Hs. 173611 NADH dehydrogenase (ubiquinone) Fe-S pro 2.86 107135 AA620782 Hs. 23247 ESTs 2.85 117748 N47317 Hs. 141858 ESTs 2.85 124030 F04143 Hs. 151032 Homo sapiens clone 23856 unknown mRNA; p 2.85 135120 AA449841 Hs. 108300 NOT3 (negative regulator of transcriptio 2.84 102156 U17977 HSU17977 Humn fibroblast cDNA H sapiens 2.84 129418 AA401401 Hs. 11127 PET112 (yeast homolog)-like 2.84 103222 X74795 Hs. 77171 minichromosome maintenance deficient (S. 2.84 125145 W38001 Accession not listed in Genbank 2.83 100560 HG2228-HT2305 Crystallin, Beta B 2.83 105370 AA238476 Hs. 22791 ESTs; Weakly similar to transmembrane pr 2.83 127036 AI468598 ESTs 2.83 128788 AA029073 Hs. 105685 ESTs 2.83 119523 W38041 Accession not listed in Genbank 2.82 126436 N31224 Hs. 211579 melanoma adhesion molecule 2.82 126559 R15866 Hs. 170263 tumor protein 53-binding protein; 1 2.82 118183 N59287 Hs. 48361 EST 2.82 101298 L40387 Hs. 118633 2′-5′oligoadenylate synthetase-like 2.81 131830 U33054 Hs. 32959 G protein-coupled receptor kinase 2 (Dro 2.81 124173 H41281 Hs. 107619 ESTs 2.81 102295 U32581 Homo sapiens KIAA0421 mRNA; partial cds 2.81 129719 N66396 Hs. 167766 ESTs; Moderately similar to Pro-a2(XI) [ 2.81 126573 AA482023 Hs. 155218 E1B-55 kDa-associated protein 5 2.81 125477 AI270093 Hs. 234642 aquaporin 3 2.81 106492 AA451896 Hs. 7922 ESTs; Weakly similar to contains similar 2.8 p19; an RNA polymerase II elongation fa 132881 T86118 Hs. 58875 ESTs 2.8 114733 AA133778 Hs. 95734 ESTs 2.79 104618 AA001611 Hs. 186494 ESTs 2.79 134137 F10045 Hs. 79347 KIAA0211 gene product 2.79 133212 U82979 Hs. 67846 leukocyte Ig-like receptor; subfamily B 2.78 100882 HG4460-HT4729 Immunoglobulin Heavy Chain, Vdjc Regions (Gb: L23564) 2.78 104756 AA024622 Hs. 15813 solute carrier family 22 (organic cation 2.78 129861 N69507 Hs. 129849 DKFZP564M182 protein 2.78 120824 AA347548 Hs. 96876 ESTs 2.78 100684 HG3107-HT3283 Plasma Membrane Calcium Pump Hpmca2a 2.78 121789 AA423970 Hs. 178111 ESTs 2.78 101847 M59941 Hs. 118200 colony stimulating factor 2 receptor; be 2.78 113722 T97957 Hs. 202948 ESTs; Weakly similar to alternatively sp 2.77 115107 AA256371 Hs. 186645 ESTs 2.77 111464 R05518 Hs. 19521 ESTs 2.77 108446 AA079120 zm95e1.s1 Stratagene colon HT29 (#937221 2.77 123921 AA621329 Hs. 250671 Hu DNA seq frm clone 1163J1 on chr 22q13 2.77 prot (similar to mouse Celsr1; rat MEGF 134445 M59488 Hs. 83384 S100 calcium-binding protein; beta (neur 2.76 114132 Z38688 Hs. 24192 ESTs 2.76 120500 AA256430 Hs. 132525 ESTs 2.76 101860 M95610 Hs. 37165 collagen; type IX; alpha 2 2.76 134430 H52105 Hs. 8309 KIAA0747 protein 2.76 124152 H27216 Hs. 107635 ESTs 2.76 132268 AA058833 Hs. 23445 ESTs; Weakly smlr to similar to M. muscu 2.76 116257 AA481493 Hs. 88537 ESTs 2.76 102438 U46570 Hs. 7733 tetratricopeptide repeat domain 1 2.75 122393 AA446334 Hs. 99064 ESTs 2.75 107653 AA010210 Hs. 47041 ESTs 2.75 123674 AA609473 Hs. 105187 ESTs; Moderately similar to kinesin like 2.75 129858 T66906 Hs. 12970 ESTs 2.75 130117 U06641 Hs. 150207 UDP glycosyltransferase 2 family; polype 2.75 133464 M13982 Hs. 73917 interleukin 4 2.75 127039 AA233366 Hs. 256491 ESTs 2.74 128318 AA418202 Hs. 13810 ESTs 2.74 123363 AA504818 Hs. 171279 ESTs 2.74 127654 AA649249 Hs. 75640 natriuretic peptide precursor A 2.74 132067 L20860 Hs. 178382 glycoprotein Ib (platelet); beta polypep 2.74 125664 AA948418 Hs. 25744 ESTs; Weakly similar to Ydr412wp [S.cere 2.73 132354 L05187 Hs. 211913 small proline-rich protein 1A 2.73 101568 M33764 Hs. 75212 ornithine decarboxylase 1 2.73 101438 M20777 Hs. 159263 Homo sapiens; alpha-2 (VI) collagen 2.73 116233 AA479082 Hs. 61142 ESTs 2.73 122194 AA435882 Hs. 97531 ESTs 2.72 113995 W88466 Hs. 22010 ESTs 2.72 124251 H68286 Hs. 107924 ESTs 2.71 120583 AA281304 Hs. 78614 complement component 1; q subcomponent b 2.71 134958 U72507 Hs. 234216 Human 40871 mRNA partial sequence 2.71 124280 H85835 Hs. 100058 dihydropyrimidinase-like 4 2.71 130113 M64673 Hs. 1499 heat shock transcription factor 1 2.71 106588 AA456612 Hs. 25682 ESTs; Weakly smlr to PHOSPHATIDYLETHANOL 2.71 132023 F01927 Hs. 3743 ESTs; Weakly similar to proline-rich pro 2.7 112284 R53558 Hs. 26052 ESTs 2.7 107897 AA026240 Hs. 61387 ESTs 2.7 122610 AA453598 Hs. 99336 ESTs 2.7 119070 R27788 Hs. 52302 ESTs 2.7 103491 Y08836 Homo sapiens mRNA for HRX-like protein 2.7 108225 AA058843 Hs. 161620 EST 2.7 105829 AA398290 Hs. 21965 ESTs 2.69 127749 AI251757 Hs. 145234 ESTs 2.69 128428 AI185718 Hs. 143900 ESTs 2.69 108409 AA075578 zm88h3.s1 Stratagene ovarian cancer (#93 2.69 114739 AA134923 Hs. 103833 ESTs; Weakly similar to predicted using 2.68 128821 D87002 Hs. 135 multiple UniGene matches 2.68 107412 W26105 Hs. 8961 ESTs 2.68 117012 H85893 Hs. 194387 ESTs; Weakly similar to !!!! ALU SUBFAMI 2.68 135262 AA416551 Hs. 9732 ESTs 2.68 105367 AA236397 Hs. 20304 ESTs 2.68 134771 L13939 Hs. 89576 adaptor-related protein complex 1; beta 2.68 105036 AA128617 Hs. 25549 ESTs 2.68 125093 T92930 Hs. 186750 ESTs 2.68 119340 T61899 Hs. 90677 ESTs; Highly similar to CGI-82 protein [ 2.67 132603 H62900 Hs. 53066 hsp70-interacting protein 2.67 113733 T98386 Hs. 184548 ESTs 2.67 123564 AA608902 Hs. 112612 ESTs 2.66 116059 AA454165 Hs. 53455 ESTs 2.66 125803 R79373 Hs. 29852 ESTs 2.66 123012 AA479962 Hs. 139636 EST 2.66 106080 AA418046 Hs. 35124 ESTs 2.66 128809 T59668 Hs. 102267 lysyl oxidase 2.66 104354 H08988 Hs. 113759 ESTs 2.66 107068 AA609028 Hs. 8032 ESTs 2.65 101418 M17754 Hs. 1276 BN51 (BHK21) temperature sensitivity com 2.65 135157 AA460138 Hs. 95582 SRY (sex-determining region Y)-box 20 2.65 123312 AA496258 Hs. 99601 ESTs 2.65 130034 C00350 Hs. 14454 chromosome 2 open reading frame 1 2.65 103897 AA248870 Hs. 55058 ESTs 2.65 117771 N47961 Hs. 46794 ESTs 2.65 109980 H09529 Hs. 98693 DKFZP586J0917 protein 2.64 121966 AA429653 Hs. 98616 EST 2.64 114233 Z39652 Hs. 27457 ESTs 2.64 129594 R70379 Hs. 115396 Human germline IgD chain gene; C-region; 2.63 102319 U34587 Hs. 66578 corticotropin releasing hormone receptor 2.63 111700 R22212 Hs. 23361 ESTs 2.63 127365 AA001628 Hs. 74335 heat shock 90 kD protein 1; beta 2.63 104205 AA496240 Hs. 17270 DKFZP434C211 protein 2.63 124559 N66223 Hs. 135928 ESTs; Weakly similar to !!!! ALU SUBFAMI 2.63 106351 AA442772 Hs. 191987 ESTs; Weakly similar to !!!! ALU SUBFAMI 2.63 121903 AA427605 Hs. 258742 myosin-binding protein C; cardiac 2.62 116442 AA620310 Hs. 184343 ESTs; Weakly similar to KIAA0585 protein 2.62 127041 F06090 HSC0WG031 normalized infant brain cDNA H 2.62 132860 U93049 Hs. 58435 FYN-binding protein (FYB-120/130) 2.62 131591 L22454 Hs. 180069 nuclear respiratory factor 1 2.61 118118 N56901 Hs. 47995 ESTs 2.61 134809 X52611 Hs. 18387 transcription factor AP-2 alpha (activat 2.61 117706 N45091 Hs. 46472 ESTs 2.61 127488 AA312179 Hs. 178617 ESTs; Weakly similar to CGI-82 protein [ 2.61 114891 AA235984 Hs. 87469 ESTs 2.6 116426 AA609668 Hs. 71657 ESTs 2.6 132589 AA432197 Hs. 5260 ESTs; Weakly similar to CGI-08 protein [ 2.6 128410 AA452788 zx39g11.r1 Soares_total_fetus_Nb2HF8_9w 2.6 106081 AA418394 Hs. 25354 ESTs 2.6 129919 R02003 Hs. 191208 ESTs; Weakly similar to weak similarity 2.59 124672 R00307 Hs. 188504 ESTs 2.59 122758 AA459013 Hs. 99742 X-ray repair complementing defective rep 2.59 125656 AA040118 Hs. 78687 neutral sphingomyelinase (N-SMase) activ 2.59 130052 J00220 Hs. 145288 Human Ig active epsilon1 5′ UT; V-D-J re 2.59 134878 U28055 Hs. 250826 macrophage stimulating; pseudogene 9 2.59 131908 L05624 Hs. 3446 mitogen-activated protein kinase kinase 2.59 126470 AA843339 Hs. 193168 ESTs; Weakly similar to CGI-52 protein [ 2.59 132353 M31651 Hs. 46319 sex hormone-binding globulin 2.58 119588 W44559 Hs. 142525 ESTs 2.58 131757 D17532 Hs. 316 DEAD/H (Asp-Glu-Ala-Asp/His) box polypep 2.58 118114 N56875 Hs. 143212 cystatin F (leukocystatin) 2.58 128200 AI279952 Hs. 158037 ESTs; Weakly similar to transcription re 2.58 131208 C14586 Hs. 24220 Homo sapiens mRNA; cDNA DKFZp566M051 (fr 2.58 124721 R11131 Hs. 154966 ESTs 2.57 108706 AA121820 Homo sapiens mRNA for KIAA0842 protein; 2.57 118831 N79592 Hs. 50838 ESTs 2.57 115708 AA412212 Hs. 44033 ESTs 2.57 107233 D59322 Hs. 22595 ESTs 2.57 129559 AA234945 Hs. 11360 ESTs 2.57 126953 AA743849 Hs. 127286 ESTs 2.56 108165 AA055221 Hs. 63168 ESTs 2.56 104069 AA401547 Hs. 172694 ESTs 2.56 112146 R46512 Hs. 25374 ESTs 2.56 108364 AA074891 Hs. 124917 ESTs; Highly similar to KIAA0838 protein 2.56 131779 R49047 Hs. 179779 ribosomal protein L37 2.56 111829 R36070 Hs. 25079 EST 2.55 103424 X97267 Hs. 155975 protein tyrosine phosphatase; receptor t 2.55 100133 D13118 Hs. 80986 ATP synthase; H+ transporting; mitochond 2.55 130208 AA620556 Hs. 15250 peroxisomal D3;D2-enoyl-CoA isomerase 2.55 124649 N92593 Hs. 102907 ESTs 2.55 106511 AA452865 Hs. 206713 UDP-Gal: betaGlcNAc beta 1;4-galactosylt 2.55 128467 AA176446 Hs. 180428 ESTs; Weakly similar to hypothetical 43. 2.55 113524 T90072 Hs. 15060 ESTs 2.55 107821 AA020991 Hs. 172856 ESTs 2.55 111900 R39044 Hs. 25318 Homo sapiens clone 25194 mRNA sequence 2.54 109908 H05255 Hs. 203237 EST 2.54 132069 D87454 Hs. 192966 KIAA0265 protein 2.54 130660 T95262 Hs. 17538 ESTs 2.54 112983 T23443 Hs. 7111 ESTs 2.54 128279 H08885 yl88b08.r1 Soares infant brain 1NIB Homo 2.54 106415 AA447994 Hs. 29188 ESTs 2.53 116741 H03268 Hs. 181746 EST 2.53 103148 X66362 Hs. 2994 PCTAIRE protein kinase 3 2.53 132336 AA342422 Hs. 45073 ESTs 2.53 129484 R92488 Hs. 111989 ESTs 2.53 110169 H19696 Hs. 31612 ESTs; Moderately similar to CAGH4 [H.sap 2.53 116880 H68380 Hs. 144174 EST 2.53 133511 X04106 Hs. 74451 calpain; small polypeptide 2.53 126037 M85772 Hs. 6066 KIAA1112 protein 2.53 132678 AA599876 Hs. 5486 ESTs 2.53 128751 AA442274 Hs. 183176 ESTs 2.52 133664 X86693 Hs. 75445 hevin 2.52 126977 AA309665 EST180547 Jurkat T-cells V Homo sapiens 2.52 120697 AA291522 Hs. 97250 EST 2.52 128571 AA416619 Hs. 101661 ESTs 2.52 104422 H86858 Hs. 132909 ESTs 2.52 122372 AA446008 Hs. 99044 EST 2.52 112154 R46769 Hs. 25388 ESTs 2.52 126900 R16034 Hs. 12701 ESTs; Highly similar to plasmolipin [H.s 2.51 115000 AA251342 Hs. 144584 ESTs 2.51 110632 H72344 Hs. 171635 ESTs 2.51 129154 N23673 Hs. 108969 mannosidase; alpha; class 2B; member 1 2.51 107440 W28069 Hs. 251993 ESTs; Weakly similar to similar to zinc 2.51 105694 AA287109 Hs. 37883 ESTs 2.51 106249 AA430388 Hs. 13144 ESTs; Weakly similar to ORF YGR038w [S.c 2.51 134462 U11037 Hs. 83620 sel-1 (suppressor of lin-12; C.elegans)- 2.51 101800 M85276 Hs. 105806 granulysin 2.51 119884 W81606 Hs. 58662 Homo sapiens mRNA; cDNA DKFZp564G212 (fr 2.51 110289 H29829 Hs. 31524 ESTs 2.51 125506 H54273 Hs. 154073 UDP-galactose transporter related 2.51 102954 X15393 Hs. 2813 motilin 2.51 127851 AI469331 Hs. 130497 ESTs; Weakly similar to CHLORIDE CONDUCT 2.5 126179 AI191445 Hs. 143855 ESTs; Highly similar to IROQUOIS-CLASS H 2.5 129443 W69967 Hs. 111497 ESTs; Moderately similar to neuronal pro 2.5 104480 N41486 Hs. 99654 protein-O-mannosyltransferase 1 2.5 115580 AA398695 Hs. 144339 Hu DNA seq frm clone 495O10 on chr 6q26- 2.5 Prot L37A) pseudogene; last exon of gene for a novel prot smlr to worm E04F6.2; ESTs; STSs and GSSs 119595 W45031 Hs. 55878 EST 2.5 103336 X85785 Hs. 183 Duffy blood group 2.5 102792 U87964 Hs. 227576 GTP binding protein 1 2.49 129643 L27584 Hs. 250712 calcium channel; voltage-dependent; beta 2.49 134503 U34880 Hs. 84183 diptheria toxin resistance protein reqrd 2.49 117245 N20989 Hs. 42927 ESTs 2.49 126888 H78745 Hs. 1063 small nuclear ribonucleoprotein polypept 2.49 135313 D63484 Hs. 98508 KIAA0150 protein 2.49 121186 AA400156 Hs. 183294 ESTs 2.49 130651 X04445 Hs. 1734 inhibin; alpha 2.49 134218 AA227480 Hs. 80205 pim-2 oncogene 2.49 104008 AA334630 EST38874 Embryo, 9 week Homo sapiens cDN 2.49 129705 X78706 Hs. 12068 camitine acetyltransferase 2.49 127900 AI143912 Hs. 121824 ESTs 2.49 104609 R96417 Hs. 107795 ESTs 2.48 131628 U47292 Hs. 2979 trefoil factor 2 (spasmolytic protein 1) 2.48 132184 U51003 Hs. 419 distal-less homeo box 2 2.48 130450 U70735 Hs. 15591 COP9 subunit 6 (MOV34 homolog; 34 kD) 2.48 101679 M62628 Hs. 163271 Human alpha-1 Ig germline C-region membr 2.48 120858 AA350147 Hs. 96940 EST 2.48 101012 J04444 Hs. 697 cytochrome c-1 2.48 110453 H52133 Hs. 33026 ESTs; Weakly similar to similar to Enter 2.48 133771 M68891 Hs. 760 GATA-binding protein 2 2.48 102944 X14445 Hs. 37092 fibroblast grwth fctr 3 (murine mammary 2.48 113269 T65159 Hs. 85044 ESTs 2.48 107069 AA609045 Hs. 11759 ESTs; Weakly similar to !!!! ALU CLASS B 2.48 100476 HG1019-HT1019 Serine Kinase Psk-H1 2.47 106457 AA449718 Hs. 27801 zinc finger protein 278 2.47 105718 AA291629 Hs. 74335 heat shock 90 kD protein 1; beta 2.47 104925 AA058683 Hs. 5548 Homo sapiens clone 23765 mRNA sequence 2.47 109913 H05527 Hs. 31588 ESTs 2.47 103412 X96698 Hs. 42957 methyltransferase-like 1 2.47 102326 U35246 Hs. 226025 vacuolar protein sorting 45A (yeast homo 2.47 116813 H49911 Hs. 93102 ESTs 2.47 123690 AA609566 Hs. 112723 EST 2.47 124714 R09486 Hs. 193118 ESTs 2.47 126154 AI004105 Hs. 14232 ESTs; Moderately similar to KIAA0563 pro 2.47 118880 N90168 Hs. 54593 EST 2.47 122274 AA437094 Hs. 184456 ESTs; Weakly similar to !!!! ALU SUBFAMI 2.46 129600 N78980 Hs. 11567 ESTs; Moderately similar to unknown [H.s 2.46 121356 AA405437 Hs. 93581 Homo sapiens mRNA; cDNA DKFZp586E171 (fr 2.46 109560 F01778 Hs. 8154 ESTs 2.46 123342 AA504336 Hs. 31659 thyroid hormone receptor-associated prot 2.46 128032 AI150084 Hs. 126678 ESTs 2.46 129101 H90310 Hs. 108665 ESTs; Weakly similar to CELL-CYCLE NUCLE 2.46 131185 M25753 Hs. 23960 cyclin B1 2.46 121451 AA411008 Hs. 98085 EST 2.46 104328 D81932 HUM424C5B Hu fetal brain (TFujiwara) H.s 2.46 126543 AA723810 Hs. 69517 ESTs; Highly similar to differentially e 2.45 123600 AA609106 Hs. 112644 ESTs 2.45 131020 AA411756 Hs. 20594 ESTs; Weakly similar to misato [D.melano 2.45 134191 W28902 Hs. 7979 KIAA0736 gene product 2.45 130446 X79510 Hs. 155693 protein tyrosine phosphatase; non-recept 2.45 131613 R88228 Hs. 29595 JM4 protein 2.45 118864 N89670 Hs. 42148 ESTs; Weakly similar to Su(P) [D.melanog 2.45 104232 AB002351 Hs. 10587 KIAA0353 protein 2.45 122604 AA453489 Hs. 99333 ESTs 2.45 120626 AA285064 Hs. 104485 EST 2.45 116655 F03866 Hs. 68090 ESTs 2.44 116267 AA485080 Hs. 256539 ESTs 2.44 114944 AA243172 Hs. 87619 TED protein 2.44 127629 AA293279 Hs. 29173 ESTs 2.44 120350 AA211300 Hs. 104166 ESTs 2.44 103620 Z47087 Hs. 182643 transcription elongation factor B (SIII) 2.44 131420 Z11737 Hs. 2664 flavin containing monooxygenase 4 2.44 131312 AA399226 Hs. 25527 tight junction protein 3 (zona occludens 2.43 122812 AA461044 Hs. 142980 EST 2.43 135100 AA398926 Hs. 251108 Homo sapiens mRNA; chromosome 1 specific 2.43 113464 T86931 Hs. 16295 ESTs 2.43 100045 M11507 AFFX control: transferrin receptor 2.43 128975 AA092129 Hs. 107538 ESTs; Moderately similar to/prediction 2.43 103688 AA011479 Hs. 154701 ESTs 2.43 127331 F20186 HSPD05873 HM3 Homo sapiens cDNA clone 05 2.43 107337 T97111 Hs. 191235 ESTs; Weakly similar to Ydr324cp [S.cere 2.43 122171 AA435750 Hs. 98830 EST 2.43 107601 AA004636 Hs. 50223 ESTs 2.43 119800 W73523 Hs. 58314 ESTs 2.43 104886 AA053348 Hs. 144626 growth differentiation factor 11 2.42 122899 AA469960 Hs. 178420 ESTs; Highly similar to WASP interacting 2.42 125933 AI308037 Hs. 84120 ESTs; Weakly similar to nucleoporin p62 2.42 121664 AA417291 Hs. 97978 ESTs 2.42 125450 AA377194 Hs. 238909 ESTs; Weakly similar to POLYPOSIS LOCUS 2.42 114611 AA081374 Hs. 108110 DKFZP547E2110 protein 2.42 111595 R11492 Hs. 191225 ESTs 2.42 111671 R19368 Hs. 229084 EST 2.42 110687 H93005 Hs. 177311 ESTs 2.42 103019 X53414 Hs. 144567 alanine-glyoxylate aminotransferase (oxa 2.42 119076 R36634 Hs. 235534 ESTs 2.42 130589 AA234308 Hs. 16441 DKFZP434H204 protein 2.42 125975 AA495891 Hs. 152290 ESTs; Highly similar to PACAP type-3/VIP 2.42 106380 AA446188 Hs. 16614 ESTs 2.41 121965 AA429652 Hs. 104901 EST 2.41 121604 AA416788 Hs. 98259 EST 2.41 100885 HG4490-HT4876 Proline-Rich Protein Prb4, Allele 2.41 117807 N48701 Hs. 46523 EST 2.41 119840 W79525 Hs. 58586 ESTs 2.41 102458 U48861 Hs. 54397 cholinergic receptor, nicotinic; beta po 2.41 116152 AA460920 Hs. 215683 ESTs; Moderately similar to !!!! ALU SUB 2.41 126741 AA522512 Hs. 29759 Homo sapiens mRNA; cDNA DKFZp586L2123 (f 2.41 103381 X92715 Hs. 3057 zinc finger protein 74 (Cos52) 2.41 124837 R55630 Hs. 233602 KIAA0596 protein 2.41 129322 AA437153 Hs. 110407 ESTs; Weakly similar to coded for by C. 2.4 129291 AA281930 Hs. 110099 core-binding factor; runt domain; alpha 2.4 124789 R43803 Hs. 78110 ESTs; Weakly similar to F17A9.2 [C.elega 2.4 133253 Y00970 Hs. 183088 acrosin 2.4 118990 N94447 Hs. 55047 EST 2.4 134897 R71427 Hs. 9081 phenylalanyl-tRNA synthetase beta-subuni 2.4 116572 D45654 Hs. 65582 DKFZP586C1324 protein 2.4 104294 D14539 Hs. 234774 myeloid/lymphoid or mixed-lineage leukem 2.4 118764 N74440 Hs. 205264 ESTs 2.4 117437 N27645 yw5e3.s1 Weizmann Olfactory Epithelium H 2.4 3′ similar to contains L1.t3 L1 repetit 111651 R16733 Hs. 20499 ESTs 2.39 109583 F02322 Hs. 26135 ESTs 2.39 125969 R94247 Hs. 193879 ESTs 2.39 130647 AA457216 Hs. 214190 interleukin enhancer binding factor 1 2.39 113708 T97487 Hs. 18065 ESTs 2.39 133469 L03785 Hs. 170482 myosin; light polypeptide 5; regulatory 2.39 118266 N62837 Hs. 48647 immunoglobulin-like transcript 7 2.39 121656 AA417248 Hs. 98212 ESTs 2.39 126530 AI422841 Hs. 180086 ESTs 2.39 123708 AA609648 Hs. 207767 EST 2.39 107875 AA025308 Hs. 61182 ESTs 2.39 111711 R22891 Hs. 7093 ESTs 2.39 131405 U79255 Hs. 26468 amyloid beta (A4) precursor protein-bind 2.39 127454 AA502957 Hs. 153590 ESTs 2.39 132341 AA448419 Hs. 45209 ESTs 2.38 133673 D87673 Hs. 75486 heat shock transcription factor 4 2.38 113213 T58607 ya94a02.s1 Stratagene placenta (#937225) 2.38 106230 AA429356 Hs. 12047 ESTs 2.38 116692 F09261 Hs. 66103 ESTs 2.38 126197 AA172284 Hs. 103657 ESTs; Weakly similar to CH-TOG PROTEIN [ 2.38 115966 AA446866 Hs. 71371 ESTs 2.38 132636 U65785 Hs. 5417 oxygen regulated protein (150 kD) 2.38 109965 H09077 Hs. 30895 EST 2.38 130203 L14754 Hs. 1521 immunoglobulin mu binding protein 2 2.38 131332 R50487 Hs. 25717 ESTs 2.38 119105 R42357 Hs. 91453 ESTs 2.37 129253 W69316 Hs. 109778 ESTs; Weakly similar to similar to beta- 2.37 113602 T92558 Hs. 17036 ESTs 2.37 118102 N55272 Hs. 145798 ESTs 2.37 100734 HG3432-HT3620 Fibroblast Growth Factor Receptor K-Sam, Alt. Splice 3, K-Sam lii 2.37 111533 R08548 Hs. 251651 EST 2.37 130813 U12259 Hs. 198 paired box gene 3 (Waardenburg syndrome 2.37 119180 R80413 Hs. 92520 ESTs 2.37 109335 AA211443 Hs. 86492 ESTs 2.37 107386 U97698 Hs. 159593 mucin 6; gastric 2.36 122486 AA448328 Hs. 115527 ESTs 2.36 112997 T23548 Hs. 167467 ESTs 2.36 109674 F09051 Hs. 21837 ESTs; Weakly similar to KIAA0927 protein 2.36 128868 AA423827 Hs. 106730 hypothetical protein 2.36 127027 R17261 yg12g07.r1 Soares infant brain 1NIB H.sa 2.36 123099 AA485931 Hs. 79 aminoacylase 1 2.36 115716 AA416767 Hs. 43498 ESTs; Weakly similar to ORF YKL201c [S.c 2.36 130830 D86982 Hs. 20060 KIAA0229 protein 2.36 109051 AA159920 Hs. 72322 ESTs 2.36 130181 R39552 Hs. 151608 Homo sapiens clone 23622 mRNA sequence 2.36 131114 R46233 Hs. 23107 ESTs 2.36 123589 AA609047 Hs. 188922 ESTs 2.36 130872 U03891 phorbolin (similar to apolipoprotein B m 2.36 131962 H78550 Hs. 2780 jun D proto-oncogene 2.36 130502 M55067 Hs. 1583 neutrophil cytosolic factor 1 (47 kD; chr 2.36 121785 AA423883 Hs. 142442 ESTs 2.35 125405 T97171 Hs. 121570 ESTs 2.35 103682 AA000993 ESTs 2.35 125649 T77395 Hs. 194816 stomatin-like protein 1 2.35 115452 AA285019 Hs. 55263 ESTs; Highly similar to mitochondrial di 2.35 129338 T56800 Hs. 47274 Homo sapiens mRNA; cDNA DKFZp564B176 (fr 2.35 106105 AA421268 Hs. 149443 putative tumor suppressor 2.35 134770 R72079 Hs. 89575 CD79B antigen (immunoglobulin-associated 2.35 119422 T99496 Hs. 229598 EST 2.35 109869 H02849 Hs. 30345 EST 2.35 134314 AA263032 Hs. 81634 ATP synthase; H+ transporting; mitochond 2.35 114989 AA251097 Hs. 189119 ESTs 2.35 122619 AA453755 Hs. 191515 ESTs 2.35 133129 AA428580 Hs. 65551 ESTs 2.35 128465 AA416762 Hs. 100221 nuclear receptor subfamily 1; group H; m 2.35 115636 AA402715 Hs. 58389 ESTs 2.35 130836 J05068 Hs. 2012 transcobalamin I (vitamin B12 binding pr 2.34 132385 Y10256 Hs. 47007 serine/threonine protein-kinase 2.34 107776 AA018820 Hs. 221147 ESTs 2.34 109791 F10669 Hs. 13228 DRE-antagonist modulator; calsenilin 2.34 124409 N33212 Hs. 107197 ESTs 2.34 131068 AA397916 Hs. 22595 ESTs 2.34 121079 AA398719 Hs. 14169 ESTs; Weakly similar to CREB-binding pro 2.34 124662 N94340 Hs. 171835 ESTs; Weakly smlr to PUT PRE-MRNA SPLICI 2.34 133820 M13686 Hs. 177582 surfactant; pulmonary-associated protein 2.34 129424 M55593 Hs. 111301 matrix metalloproteinase2 (gelatinase A 2.34 109066 AA161377 Hs. 72404 EST 2.34 100339 D63485 Hs. 181359 KIAA0151 gene product 2.34 100809 HG3991-HT4261 Cpg-Enriched Dna, Clone E18 2.34 120844 AA349417 Hs. 96917 ESTs 2.33 124927 R96146 Hs. 221459 ESTs 2.33 109779 F10527 Hs. 3353 Homo sapiens clone 24940 mRNA sequence 2.33 101171 L16842 Hs. 119251 ubiquinol-cytochrome c reductase core pr 2.33 110805 N26904 Hs. 24048 ESTs; Weakly similar to FK506/rapamycin- 2.33 125440 AI090982 Hs. 31895 ESTs 2.33 133159 AC000061 Hs. 663 cystic fibrosis transmemb conductance re 2.33 101829 M91368 Hs. 129763 solute carrier family 8 (sodium/calcium 2.33 126492 AA778565 Hs. 142505 ESTs 2.33 102774 U83303 Hs. 164021 small inducible cytokine subfamily B (CX 2.33 130480 N50809 Hs. 15760 ESTs; Weakly similar to similar to Yeast 2.33 126878 AI424759 Hs. 238928 ESTs 2.33 117338 N23889 Hs. 43466 ESTs 2.32 118662 N70877 Hs. 13055 ESTs 2.32 130354 AA416685 Hs. 155001 UNC13 (C. elegans)-like 2.32 106760 AA477330 Hs. 12293 ESTs 2.32 124294 H90573 Hs. 102298 EST 2.32 119428 W02129 Hs. 55242 EST 2.32 132629 Z40942 Hs. 5383 ESTs 2.32 127998 AA854161 Hs. 143585 ESTs 2.32 132728 AA293334 Hs. 5566 ESTs; Highly similar to RAS-RELATED PROT 2.32 120292 AA189116 Hs. 96168 ESTs 2.32 107598 AA004528 Hs. 169444 ESTs 2.32 128164 AI478174 Hs. 144846 ESTs 2.32 105753 AA299789 Hs. 15277 ESTs 2.31 131256 AA262340 Hs. 24907 coronin; actin-binding protein: 2B 2.31 110891 N38863 Hs. 234392 platelet-activating factor acetylhydrola 2.31 116767 H13689 Hs. 92530 ESTs 2.31 100545 HG2147-HT2217 Mucin 3, Intestinal (Gb: M55405) 2.31 125264 W88995 Hs. 167641 ESTs; Weakly similar to C15H9.5 [C.elega 2.31 118387 N64579 yz51d11.s1 Morton Fetal Cochlea H.sapien 2.31 104335 D83847 Hs. 183864 elastase 3B 2.31 107464 W42944 Hs. 171939 ESTs 2.31 112304 R54798 Hs. 26239 ESTs 2.31 134313 AA136100 Hs. 6673 trinucleotide repeat containing 15 2.31 116322 AA490900 Hs. 58643 ESTs; Highly similar to JAK3B [H. sapiens 2.31 111275 N70970 Hs. 35006 ESTs 2.31 100109 AJ000480 Hs. 143513 phosphoprotein regulated by mitogenic pa 2.31 109338 AA211717 Hs. 86507 ESTs 2.31 134432 AA053022 Hs. 8312 ESTs 2.31 129649 AD000092 Hs. 182628 Homo sapiens DNA from chr 19p13.2 cosmid 2.31 EKLF; GCDH; CRTC; and RAD23A genes; gen 122623 AA453990 Hs. 99248 ESTs 2.31 112070 R43976 Hs. 236310 EST 2.31 127683 AA668123 Hs. 134170 ESTs 2.31 104920 AA057620 Hs. 30807 ESTs; Highly similar to dJ186O1.1 [H.sap 2.31 106064 AA417373 Hs. 15898 ESTs 2.31 106782 AA478487 ESTs 2.31 126709 AA028159 Hs. 47234 ESTs 2.3 105129 AA158386 Hs. 186476 ESTs 2.3 105719 AA291644 Hs. 36793 ESTs 2.3 121698 AA418399 Hs. 10351 KIAA0308 protein 2.3 119069 R27619 Hs. 231046 EST 2.3 130388 U72515 Hs. 189583 putative protein similar to nessy (Droso 2.3 103444 X98801 Hs. 74617 dynactin 1 (p150; Glued (Drosophila) hom 2.3 114604 AA076128 zm18g4.s1 Stratagene pancreas (#93728) H 2.3 3′ similar to SW: RS1A_HUMAN P3927 4S RI 2.3 103878 AA227635 Hs. 202588 ESTs 2.3 105828 AA398276 Hs. 11962 ESTs 2.3 119778 W72920 Hs. 58244 ESTs 2.3 120401 AA234309 Hs. 193011 ESTs 2.3 116290 AA488691 Hs. 57969 phenylalanine-tRNA synthetase 2.3 130479 R44163 Hs. 12457 Homo sapiens clone 23770 mRNA sequence 2.3 104253 AF002672 Hs. 152944 loss of heterozygosity; 11; chromosomal 2.29 132615 H66367 Hs. 53358 ESTs; Weakly similar to !!!! ALU SUBFAMI 2.29 121954 AA429598 Hs. 98587 ESTs 2.29 101336 L49169 Hs. 75678 FBJ murine osteosarcoma viral oncogene h 2.29 127247 AA313802 Hs. 6289 growth factor receptor-bound protein 2 2.29 117300 N22565 Hs. 43212 ESTs 2.29 122229 AA436198 Hs. 103902 ESTs 2.29 125106 T95766 Hs. 189760 ESTs 2.29 128083 R16100 Hs. 166476 ESTs 2.29 131279 AA089853 Hs. 25197 STIP1 homology and U-Box containing prot 2.29 133838 M97796 Hs. 180919 inhibitor of DNA binding 2; dominant neg 2.29 111837 R36447 Hs. 24453 ESTs 2.29 111435 R01620 Hs. 19198 ESTs 2.29 123613 AA609158 Hs. 112656 EST 2.29 133560 AA256365 Hs. 7486 protein expressed in thyroid 2.29 122896 AA469952 Hs. 97899 ESTs; Weakly similar to dal2; len: 343; C 2.29 113378 T80627 Hs. 14757 ESTs 2.29 127174 AA293204 Hs. 139352 ESTs 2.29 120153 Z39582 Hs. 65777 EST 2.29 112741 R93080 Hs. 35035 ESTs 2.28 132152 AA044784 Hs. 4105 Homo sapiens mRNA; cDNA DKFZp586A0618 (f 2.28 109790 F10665 Hs. 25031 ESTs 2.28 113776 W04657 Hs. 24248 ESTs 2.28 102934 X13451 Hu mRNA for lymphocyte lineage-rstrcted 2.28 126188 AA322034 EST24690 Cerebellum II Homo sapiens cDNA 2.28 126363 N94706 Human Chromosome 16 BAC clone CIT987SK-A 2.28 101427 M19508 Human myeloperoxidase gene, exons 1-4 2.28 132616 AA386264 Hs. 5337 isocitrate dehydrogenase 2 (NADP+); mito 2.28 105537 AA258813 Hs. 27160 ESTs 2.28 126527 AA548559 Hs. 103853 ESTs 2.28 115359 AA281936 Hs. 88914 ESTs 2.28 108474 AA079667 zm93d1.s1 Stratagene ovarian cncr (#9372 2.28 120685 AA291066 Hs. 105099 ESTs 2.28 126171 AA704771 Hs. 191942 ESTs 2.28 112858 T02963 Hs. 4454 ESTs 2.28 121817 AA424826 Hs. 98475 EST 2.28 107895 AA026150 Hs. 61384 ESTs 2.28 131161 Z38223 Hs. 23735 potassium voltage-gated channel; subfami 2.28 135173 M72885 Hs. 95910 Human G0S2 protein gene; complete cds 2.27 103182 X69819 Hs. 99995 intercellular adhesion molecule 3 2.27 113889 W72720 Hs. 194347 ESTs 2.27 128984 AA319615 Hs. 238030 secretory carrier membrane protein 2 2.27 101531 M29877 Hs. 576 fucosidase; alpha-L-1; tissue 2.27 115916 AA436889 Hs. 91910 ESTs 2.27 129892 H96850 Hs. 89674 dolichyl-diphosphooligosaccharide-protei 2.27 103035 X54871 Hs. 77690 RAB5B; member RAS oncogene family 2.27 126479 T78141 ESTs 2.27 125778 R71976 Hs. 161791 ESTs; Weakly similar to !!!! ALU SUBFAMI 2.27 108132 AA053586 Hs. 63048 ESTs 2.27 111017 N53965 Hs. 256327 ESTs 2.27 127165 AA359719 Hs. 127121 ESTs 2.27 126446 AI421309 Hs. 118926 DKFZP586K0919 protein 2.26 107864 AA025061 Hs. 61246 ESTs 2.26 122277 AA437133 Hs. 98936 ESTs 2.26 115604 AA400378 Hs. 49391 ESTs 2.26 105061 AA134824 Hs. 4865 ESTs 2.26 118549 N68163 Hs. 49455 EST 2.26 110509 H56493 Hs. 61960 ESTs; Moderately similar to HYPOTHETICAL 2.26 114088 Z38280 Hs. 26971 Human Chromosome 16 BAC clone CIT987SK-2 2.26 103225 X74837 Hs. 2750 mannosidase; alpha; class 1A; member 1 2.26 125842 AA746654 Hs. 5181 proliferation-associated 2G4; 38 kD 2.26 104538 R25069 Hs. 175681 ESTs 2.26 130304 U09368 Hs. 154205 zinc finger protein 140 (clone pHZ-39) 2.26 120680 AA290743 Hs. 97242 ESTs 2.26 124062 H00440 Hs. 144524 ESTs; Weakly similar to signal transduce 2.26 103289 X80915 Hs. 1573 growth differentiation factor 5 (cartila 2.26 109286 AA197273 Hs. 191324 ESTs 2.26 128555 U62739 Hs. 101408 branched chain aminotransferase 2; mitoc 2.26 129439 AA171694 Hs. 111461 ceruloplasmin (ferroxidase) 2.26 109221 AA192755 Hs. 85840 ESTs; Weakly similar to stac [H. sapiens] 2.26 109906 H05084 Hs. 28077 ESTs; Highly similar to GDP-mannose pyro 2.26 130540 U35234 Hs. 159534 protein tyrosine phosphatase; receptor t 2.26 122870 AA405158 Hs. 192861 Spi-B transcription factor (Spi-1/PU.1 r 2.26 120219 Z41124 Hs. 66045 EST 2.26 128021 AI001136 Hs. 78223 N-acylaminoacyl-peptide hydrolase 2.26 121732 AA421047 Hs. 98330 ESTs 2.26 107817 AA020781 Hs. 60847 ESTs 2.25 101069 L02648 Hs. 84232 transcobalamin II; macrocytic anemia 2.25 103065 X58399 Hs. 81221 Human L2-9 transcript of unrearranged im 2.25 118019 N52585 Hs. 47517 ESTs 2.25 122220 AA436011 Hs. 98187 ESTs 2.25 109161 AA179392 Hs. 73601 EST 2.25 128699 K03207 Hs. 103972 proline-rich protein BstNI subfamily 4 2.25 101914 S71824 Hs. 167988 neural cell adhesion molecule 1 2.25 102697 U74667 Hs. 6364 Tat interactive protein (60 kD) 2.25 119939 AA86753 Hs. 82407 ESTs 2.25 127793 AI298835 Hs. 30445 ESTs; Weakly similar to transcription re 2.25 104450 L77564 Hs. 103978 serine/threonine kinase 22B (spermiogene 2.25 133096 AA136042 Hs. 131053 ESTs 2.25 115416 AA283893 Hs. 203866 ESTs 2.25 117058 H90322 Hs. 41387 EST 2.25 115598 AA400129 Hs. 65735 ESTs 2.25 121267 AA401397 Hs. 165296 ESTs; Highly similar to kallikrein-like 2.25 104778 AA026397 Hs. 11039 Homo sapiens clone 24804 mRNA sequence 2.25 110926 N48252 Hs. 135287 ESTs 2.24 102795 U88667 Hs. 198396 ATP-binding cassette; sub-family A (ABC1 2.24 118643 N70324 Hs. 49840 ESTs 2.24 103304 X82240 Hs. 2484 T-cell leukemia/lymphoma 1A 2.24 134814 Z48475 Hs. 89771 glucokinase (hexokinase 4) regulatory pr 2.24 125912 AA171719 Hs. 5233 eukaryotic translation initiation factor 2.24 134365 R32377 Hs. 82240 syntaxin 3A 2.24 117224 N20300 Hs. 218707 ESTs 2.24 107169 AA621601 Hs. 184446 ESTs; Weakly similar to small GTP-bindin 2.24 133948 M59916 Hs. 77813 sphingomyelin phosphodiesterase 1; acid 2.24 101426 M19483 Hs. 25 ATP synthase; H+ transporting; mitochond 2.24 119922 W86196 Hs. 177384 ESTs 2.24 123361 AA504810 Hs. 139649 EST 2.24 123915 AA621298 Hs. 112967 ESTs 2.24 123540 AA608792 Hs. 112591 EST 2.24 124978 T40560 Hs. 221759 ESTs 2.24 102354 U38268 Human cytochrome b pseudogene, partial c 2.24 124198 H53099 Hs. 198271 NADH dehydrogenase (ubiquinone) 1 alpha 2.24 102160 U18235 Hs. 121561 ATP-binding cassette; sub-family A (ABC1 2.24 107520 X76091 Hs. 100007 regulatory factor X; 2 (influences HLA c 2.24 131589 U52100 Hs. 29191 epithelial membrane protein 2 2.24 126633 AA206993 Hs. 154145 guanine nucl binding protein (G protein) 2.23 130887 AA258379 Hs. 155986 angiotensin receptor-like 2 2.23 119894 W84670 Hs. 58518 EST 2.23 124544 N63837 Hs. 40500 similar to S. cerevisiae RER1 2.23 103104 X61587 Hs. 75082 ras homolog gene family; member G (rho G 2.23 110119 H17306 Hs. 177229 ESTs 2.23 131411 AA464043 Hs. 26506 ESTs; Weakly similar to NY-REN-45 antige 2.23 102346 U37359 Hs. 227297 meiotic recombination (S. cerevisiae) 11 2.23 106003 AA411167 Hs. 8734 ESTs; Moderately similar to !!!! ALU CLA 2.23 122564 AA452251 Hs. 98669 ESTs 2.23 133688 U42031 Hs. 7557 FK506-binding protein 5 2.23 132096 AA131410 Hs. 3964 Homo sapiens clone 24877 mRNA sequence 2.23 110038 H11746 Hs. 31097 ESTs 2.23 123788 AA620293 Hs. 112853 ESTs 2.23 135070 X99350 Hs. 93974 forkhead box J1 2.23 104908 AA055841 Hs. 154396 ESTs 2.22 128674 AA025001 Hs. 169452 ESTs 2.22 100810 HG3992-HT4262 Cpg-Enriched Dna, Clone E35 2.22 120065 W93579 Hs. 59478 EST 2.22 122775 AA459692 Hs. 112143 ESTs 2.22 125443 H71482 Hs. 177592 tibosomal protein; large; P1 2.22 118617 N69666 Hs. 183413 ESTs; Moderately similar to !!!! ALU SUB 2.22 128001 AI167814 Hs. 166664 ESTs 2.22 128160 AI279080 Hs. 149971 ESTs; Moderately similar to !!!! ALU CLA 2.22 106608 AA458644 Hs. 27115 ESTs 2.22 103485 Y08409 Hs. 248415 thyroid hormone responsive SPOT14 (rat) 2.22 135008 AA173423 Hs. 92918 ESTs; Weakly similar to R07G3.8 [C.elega 2.22 110122 H17333 Hs. 159837 EST 2.22 128397 AI393421 Hs. 14032 ESTs 2.22 110231 H24359 Hs. 28733 ESTs 2.22 123188 AA489092 Hs. 177726 ESTs 2.22 131903 AA481723 Hs. 3436 deleted in oral cancer (mouse; homolog) 2.22 122649 AA454616 Hs. 90336 ATPase; H+ transporting; lysosomal (vacu 2.22 133090 AA448228 Hs. 6468 ESTs 2.22 108002 AA037664 Hs. 55067 ESTs; Weakly similar to T07F12.1 gene pr 2.22 133120 X64559 Hs. 65424 tetranectin (plasminogen-binding protein 2.21 114263 Z40073 Hs. 6045 ESTs 2.21 125518 R20148 Hs. 193851 ESTs 2.21 128613 U78551 Hs. 102482 Homo sapiens gallbladder mucin MUC5B mRN 2.21 102773 U83192 Hs. 23731 discs; large (Drosophila) homolog 4 2.21 119526 W38049 Accession not listed in Genbank 2.21 126844 AA299325 EST11903 Uterus tumor I Homo sapiens cDN 2.21 105860 AA399251 Hs. 180933 ESTs; Weakly similar to methyl-CpG bindi 2.21 126957 AA733145 Hs. 194560 ESTs 2.21 108959 AA150107 Hs. 81810 ESTs 2.2 131663 AA423926 Hs. 30318 ESTs 2.2 127468 H02941 Hs. 8888 ESTs 2.2 104483 N42776 Hs. 146233 EST 2.2 123848 AA620773 Hs. 221996 ESTs 2.2 101623 M55905 Hs. 75342 malic enzyme 2; NAD(+)-dependent; mitoch 2.2 120872 AA357993 Hs. 96996 ESTs 2.2 135033 AA173241 Hs. 93454 ESTs 2.2 122286 AA437259 Hs. 104944 EST 2.2 114862 AA235174 Hs. 50250 ESTs 2.2 100255 D38047 Hs. 78466 proteasome (prosome; macropain) 26S subu 2.2 103063 X58234 Hs. 123178 translocase of inner mitochondrial membr 2.2 132777 R56898 Hs. 56663 ESTs 2.2 133082 AA457129 Hs. 6455 RuvB (E. coli homolog)-like 2 2.2 127529 AA558980 Hs. 191750 ESTs 2.2 114602 AA075642 Hs. 103594 deleted in malignant brain tumors 1 2.2 120722 AA293435 Hs. 97277 ESTs 2.2 102675 U72512 Human B-cell receptor associated protein 2.2 128551 H09058 Hs. 237323 N-acetylglucosamine-phosphate mutase; DK 2.2 112020 R43001 Hs. 22298 EST 2.2 123625 AA609216 Hs. 112666 EST 2.2 120315 AA194266 Hs. 178393 ESTs 2.2 122081 AA431992 Hs. 104920 ESTs 2.19 101798 M85220 Accession not listed in Genbank 2.19 111501 R07444 Hs. 163118 ESTs 2.19 132832 D63482 Hs. 57734 KIAA0148 gene product 2.19 100544 HG2147-HT2217 Mucin 3, Intestinal (Gb: M55405) 2.19 106835 AA482077 Hs. 33713 ESTs; Weakly similar to hypothetical pro 2.19 132934 AA076145 Hs. 61053 ESTs 2.19 108762 AA127515 Hs. 71787 ESTs; Highly similar to 30S ribosomal pr 2.19 120164 Z39733 Hs. 158159 FAT tumor suppressor (Drosophila) homolo 2.19 135395 L08096 Hs. 99899 tumor necrosis factor (ligand) superfami 2.19 101717 M69013 Hs. 1686 guanine nucleotide binding protein (G pr 2.19 121172 AA400013 Hs. 97750 EST 2.18 114861 AA235123 Hs. 40719 ESTs 2.18 120851 AA349662 Hs. 174248 ESTs 2.18 121083 AA398736 Hs. 97653 EST 2.18 107171 AA621624 Hs. 28088 Homo sapiens clone 24515 mRNA sequence 2.18 128754 D31446 Hs. 10488 Breakpoint cluster region protein; uteri 2.18 100149 D13897 Hs. 169249 peptide YY 2.18 132405 AA323787 Hs. 4770 KIAA1068 protein 2.18 114666 AA112274 zm27g6.s1 Stratagene pancreas (#93728) H 2.18 element; contains element LTR8 repetitiv 127008 AA223879 zr10g05.r1 Stratagene NT2 neuronal precu 2.18 110373 H42896 Hs. 29438 ESTs 2.18 119354 T66942 Hs. 100651 golgi SNAP receptor complex member 2 2.18 130115 M31627 Hs. 149923 X-box binding protein 1 2.18 130514 AA161085 Hs. 15871 ESTs; Weakly similar to acid phosphatase 2.18 128848 H08077 Hs. 217179 ESTs; Weakly similar to T27A1.5 [C.elega 2.18 110161 H19312 Hs. 28096 ESTs 2.18 132367 X82224 Hs. 46634 cysteine conjugate-beta lyase; cytoplasm 2.18 125882 H45538 Hs. 101448 metastasis associated 1 2.17 113837 W57698 Hs. 8888 ESTs 2.17 106376 AA444004 Hs. 6084 ESTs 2.17 113755 T99075 Hs. 18570 ESTs 2.17 107525 X91817 Hs. 102866 transketolase-like 1 2.17 119207 R93186 Hs. 84298 CD74 antigen (invar polypept of maj hist 2.17 131862 AA236365 3-phosphoglycerate dehydrogenase 2.17 115514 AA297739 Hs. 55609 ESTs; Weakly similar to ISOLEUCYL-TRNA S 2.17 112290 R53940 Hs. 26016 ESTs 2.17 126136 H83353 yv82f02.r1 Soares melanocyte 2NbHM Homo 2.17 121574 AA412712 Hs. 119325 Huntingtin-interacting protein A 2.17 118530 N67900 Hs. 118446 ESTs 2.16 132327 AA203285 Hs. 44892 ESTs; Weakly similar to dJ733D15.1 [H.sa 2.16 100564 HG2239-HT2324 Potassium Channel Protein (Gb: Z11585) 2.16 129376 AA022622 Hs. 13543 ESTs; Weakly similar to hypothetical pro 2.16 135317 X86012 Hs. 98602 Human DNA sequence from intron 22 of the 2.16 9.5 kb repeated region; int22h-1; involv 114973 AA250845 Hs. 87762 ESTs 2.16 107559 AA001504 Hs. 59860 ESTs 2.16 111014 N53787 Hs. 191117 ESTs 2.16 101250 L34060 Hs. 79133 cadherin 8 2.16 110697 H93721 Hs. 20798 ESTs 2.16 126843 AA450166 Hs. 22641 ESTs; Moderately similar to predicted pr 2.16 108272 AA063616 Hs. 43773 ESTs 2.16 125012 T66935 Hs. 104859 ESTs 2.16 111639 R16101 Hs. 140834 EST 2.15 123157 AA488443 Hs. 100426 DKFZP564A063 protein 2.15 102315 U34252 Hs. 2533 aldehyde dehydrogenase 9 (gamma-aminobut 2.15 131897 AA287623 Hs. 3426 GTPase; human homolog of E. coli essenti 2.15 121528 AA412253 Hs. 238909 ESTs; Weakly similar to POLYPOSIS LOCUS 2.15 122806 AA460707 Hs. 106397 ESTs 2.15 125727 H00958 Hs. 181641 ESTs 2.15 133279 AA069571 Hs. 6957 Homo sapiens clone 24616 mRNA sequence 2.15 103219 X74570 Hs. 75268 sialyltransferase 4C (beta-galactosidase 2.15 120881 AA362144 Hs. 104601 EST 2.15 134060 D42039 Hs. 78871 KIAA0081 protein 2.15 106598 AA457140 Hs. 11411 DKFZP566O084 protein 2.15 125576 R66208 yi30h03.r1 Soares placenta Nb2HP H sapie 2.15 contains Alu repetitive element; contain 126727 AA037230 Hs. 135084 cystatin C (amyloid angiopathy and cereb 2.15 101490 M25629 Hs. 123107 kallikrein 1; renal/pancreas/salivary 2.15 129708 AA417181 Hs. 120858 ESTs 2.14 100627 HG2702-HT2798 Serine/Threonine Kinase (Gb: Z25424) 2.14 121703 AA418671 Hs. 104807 ESTs 2.14 106809 AA479704 Hs. 220324 Humn DNA seq frm clone 283E3 on chr 1p36 2.14 Female Reproductive tract MIFR1; -2; MM 129525 F03873 Hs. 112306 Homo sapiens clone 24955 mRNA sequence; 2.14 100478 HG1067-HT1067 Mucin (Gb: M22406) 2.14 118593 N69020 Hs. 207689 EST 2.14 114047 W94427 Hs. 3807 ESTs; Weakly similar to PHOSPHOLEMMAN PR 2.14 128823 AA478207 Hs. 10632 ESTs; Moderately similar to sex-determin 2.14 100534 HG1980-HT2023 Tubulin, Beta 2 2.14 105757 AA321146 Hs. 30596 ESTs 2.14 109617 F03192 Hs. 26789 ESTs; Weakly similar to dJ162H14.1 [H.sa 2.14 121547 AA412448 Hs. 104777 ESTs 2.14 119420 T98291 Hs. 102484 glutathione S-transferaseA3 2.14 120274 AA177051 nc02a02.s1 NCI_CGAP_Pr3 Homo sapiens cDN 2.14 repetitive element;contains element LTR 132933 AA598702 Hs. 6101 bone morphogenetic protein 6 2.14 133405 X07881 Hs. 73031 proline-rich protein BstNI subfamily 3 2.14 119811 W73922 Hs. 49047 ESTs 2.14 134536 AA457735 Hs. 850 IMP (inosine monophosphate) dehydrogenas 2.14 105125 AA157799 Hs. 6980 aldo-keto reductase family 7; member A2 2.14 101398 M15881 Hs. 1137 uromodulin (uromucoid;Tamm-Horsfall gly 2.14 132751 AA397901 Hs. 55993 ESTs 2.13 115777 AA424142 Hs. 39384 putative secreted ligand homologous to f 2.13 123193 AA489228 Hs. 136956 ESTs 2.13 116875 H67749 Hs. 161022 EST 2.13 107271 D60607 Hs. 34931 EST 2.13 134551 R44839 Hs. 8526 i-beta-1; 3-N-acetylglucosaminyltransfera 2.13 113413 T83739 Hs. 186512 ESTs 2.13 120522 AA258843 Hs. 258748 ESTs 2.13 119965 W87738 Hs. 59039 EST 2.13 131283 AA101601 Hs. 183986 herpesvirus entry mediator B (poliovirus 2.13 107347 U43628 Hs. 102598 mucosal vascular addressin cell adhesion 2.13 116490 C14265 Hs. 66450 ESTs 2.13 100563 HG2239-HT2324 Potassium Channel Protein (Gb: Z11585) 2.13 110441 H50302 Hs. 19845 ESTs; Highly similar to protein phosphat 2.13 101035 J05158 Hs. 73858 carboxypeptidase N; polypeptide 2; 83 kD 2.13 132500 AA047297 Hs. 50107 ESTs; Moderately similar to CDO [H.sapie 2.13 129807 L34820 Hs. 5299 aldehyde dehydrogenase 5 family; member 2.13 106250 AA430466 Hs. 28890 ESTs 2.13 113569 T91086 Hs. 162070 EST 2.13 122911 AA470087 Hs. 239726 ESTs 2.13 107452 W28988 Hs. 250746 ESTs 2.12 111824 R35661 Hs. 25006 EST 2.12 132831 U53442 Hs. 57732 mitogen-activated protein kinase 11 2.12 110244 H26742 Hs. 25367 ESTs; Weakly similar to ALR [H. sapiens] 2.12 128918 H85347 Hs. 107164 spectrin; beta; non-erythrocytic 1 2.12 133728 M10901 Hs. 75772 nuclear receptor subfamily 3; group C; m 2.12 122476 AA448211 Hs. 99164 ESTs 2.12 132004 L37360 Hs. 37054 ephrin-A3 2.12 113971 W86760 Hs. 220682 ESTs 2.12 103386 X92972 Hs. 80324 protein phosphatase 6; catalytic subunit 2.12 131120 AA443676 Hs. 23133 ESTs; Weakly similar to alcohol sulfotra 2.12 102186 U20285 G protein pathway suppressor 1 2.12 103694 AA018541 Hs. 60580 zinc finger protein 2.12 111995 R42333 Hs. 20893 ESTs 2.12 124436 N39596 Hs. 182584 ESTs 2.12 100306 D50495 Hs. 80598 transcription elongation factor A (SII); 2.12 103084 X59932 Hs. 77793 c-src tyrosine kinase 2.11 115092 AA255903 Hs. 80975 CD39-like 4 2.11 121579 AA416543 Hs. 111981 ESTs 2.11 127101 AI349351 Hs. 118944 ESTs 2.11 121195 AA400273 Hs. 97791 ESTs 2.11 112721 R91484 Hs. 30853 ESTs 2.11 113253 T64207 Hs. 55296 HLA-B associated transcript-1 2.11 120838 AA348887 Hs. 96907 ESTs 2.11 114122 Z38582 Hs. 12751 ESTs 2.11 112635 R82298 Hs. 29497 ESTs 2.11 103785 AA095600 Hs. 225647 ESTs 2.11 128260 AA331445 EST35277 Embryo, 8 week I Homo sapiens c 2.11 122987 AA479155 Hs. 103364 ESTs 2.11 110374 H42983 Hs. 227263 ESTs 2.11 116595 D60625 Hs. 177656 calmodulin 1 (phosphorylase kinase; delt 2.11 126117 H78617 yu26a08.r1 Soares fetal liver spleen 1NF 2.11 116610 D80448 Hs. 45177 ESTs 2.11 111430 R01248 Hs. 19165 ESTs 2.11 106700 AA463929 Hs. 28701 ESTs 2.11 120181 Z40121 Hs. 65870 ESTs; Weakly similar to Pro-Pol-dUTPase 2.1 132545 AA147218 Hs. 5105 ESTs 2.1 105005 AA115253 Hs. 28805 ESTs 2.1 126702 U54602 Hs. 2785 keratin 17 2.1 124096 H10060 Hs. 101687 EST 2.1 132720 Z69881 Hs. 5541 ATPase; Ca++ transporting; ubiquitous 2.1 121926 AA428559 Hs. 104895 ESTs 2.1 125734 AA157445 Hs. 227391 DKFZP547E1010 protein 2.1 122368 AA443963 Hs. 104964 EST 2.1 116910 H72014 Hs. 161031 ESTs; Weakly similar to SYNAPTOTAGMIN I 2.1 113171 T54613 Hs. 9761 EST 2.1 134629 U00951 Hs. 87150 Human clone A9A2BR11 (CAC)n/(GTG)n repea 2.1 105712 AA291293 Hs. 25219 ESTs 2.1 106931 AA495918 Hs. 26714 ESTs 2.1 114278 Z40424 Hs. 27728 ESTs 2.1 116615 D80666 Hs. 45203 ESTs 2.09 100189 D21089 Hs. 320 xeroderma pigmentosum; complementation g 2.09 119500 W37694 Hs. 55561 ESTs 2.09 129605 S72493 Hs. 115947 keratin 16 (focal non-epidermolytic palm 2.09 133912 X62744 Hs. 77522 major histocompatibility complex; class 2.09 129636 N34942 Hs. 11782 ESTs 2.09 106372 AA443941 Hs. 4992 tumor suppressing subtransferable candid 2.09 101885 M98539 Hs. 8272 prostaglandin D2 synthase (21 kD; brain) 2.09 132749 AA235989 Hs. 55967 short stature homeobox 2 2.09 135042 X91348 Hs. 93522 putative non-coding transcript (DiGeorge 2.09 109404 AA224594 Hs. 86941 ESTs 2.09 101333 L47738 Hs. 80313 p53 inducible protein 2.09 100114 D00596 Hs. 82962 thymidylate synthetase 2.09 130536 T17045 Hs. 159492 spastic ataxia of Charlevoix-Saguenay (s 2.09 125772 R83903 Hs. 78040 KDEL (Lys-Asp-Glu-Leu) endoplasmic retic 2.09 132192 AA247569 Hs. 4209 ESTs 2.09 124697 R06273 Hs. 186467 ESTs; Moderately similar to !!!! ALU SUB 2.09 127694 AI247780 Hs. 117036 ESTs 2.08 127895 AA772600 Hs. 187998 ESTs; Weakly similar to ATP-binding cass 2.08 121315 AA402883 Hs. 82269 progestagen-associated endometrial prote 2.08 endometrial alpha-2-globulin; alpha ute 112150 R46576 Hs. 23239 ESTs 2.08 105054 AA133584 Hs. 26333 JM1 protein 2.08 113151 T51620 Hs. 9326 EST 2.08 118783 N75285 Hs. 50593 ESTs; Moderately similar to cytoplasmic 2.08 126748 AA249580 Hs. 239975 ESTs; Moderately similar to CDO [H.sapie 2.08 135160 U77643 Hs. 95655 secreted and transmembrane 1 2.08 107518 X60152 zinc finger protein 2 2.08 126055 N28990 yx39g04.r1 Soares melanocyte 2NbHM Homo 2.08 116982 H81933 Hs. 40317 ESTs 2.08 101756 M77235 Hs. 169331 sodium channel; voltage-gated; type V; a 2.08 116935 H75763 Hs. 53468 ESTs 2.08 118556 N68408 Hs. 194637 Homo sapiens mRNA; cDNA DKFZp564D113 (fr 2.08 129812 L07807 Hs. 166161 dynamin 1 2.08 121946 AA429411 Hs. 104888 ESTs 2.08 133843 AA489045 Hs. 76691 Homo sapiens clone 25100 mRNA sequence; 2.08 122170 AA435744 Hs. 163913 ESTs 2.08 122399 AA446449 Hs. 231112 EST 2.08 105775 AA348274 Hs. 6664 ESTs 2.08 123943 AA621553 Hs. 112998 ESTs 2.08 105771 AA347967 Hs. 256267 neuroblastoma RAS viral (v-ras) oncogene 2.08 114454 AA021091 Hs. 226208 ESTs 2.08 125802 R78852 Hs. 151099 ESTs 2.08 131556 AA442853 Hs. 2869 cyclin-dependent kinase 5; regulatory su 2.08 118837 N79836 Hs. 216338 ESTs 2.08 107345 U26209 Hs. 102307 solute carrier family 13 (sodium-depende 2.08 131324 H58690 Hs. 25625 ESTs 2.08 105233 AA216759 Hs. 191132 ESTs 2.07 112886 T03864 Hs. 7436 putative acyltransferase 2.07 120252 AA169400 Hs. 152701 DKFZP434F124 protein 2.07 114867 AA235310 Hs. 52899 ESTs; Moderately similar to !!!! ALU SUB 2.07 106715 AA464955 Hs. 126062 ESTs; Weakly similar to EPIDERMAL GROWTH 2.07 125560 R51281 Hs. 13692 ESTs; Highly similar to PROTEIN TSG24 [M 2.07 112270 R53021 Hs. 203358 ESTs 2.07 134626 S82198 Hs. 8709 caldecrin (serum calcium decreasing fact 2.07 115723 AA417345 Hs. 54846 ESTs 2.07 123895 AA621192 Hs. 112949 EST 2.07 119906 W85818 ESTs; Moderately similar to !!!! ALU SUB 2.07 108559 AA085161 zn12c5.s1 Stratagene hNT neuron (#937233 2.07 IMAGE: 54728 3′ similar to TR: G1151228 G 101246 L33799 Hs. 202097 procollagen C-endopeptidase enhancer 2.07 100663 HG2915-HT3059 Major Histocompatibility Complex, Class I, E (Gb: M20022) 2.07 114178 Z39063 Hs. 17930 Humn DNA seq frm clone 1033B10 on chr 6p 2.07 for GalT3 (beta3-Galactosyltransferase) 125672 AA152281 Hs. 78601 uroporphyrinogen decarboxylase 2.07 118052 N53360 Hs. 165133 ESTs 2.07 102387 U41163 Hs. 229731 solute carrier family 6 (neurotransmitte 2.07 127305 AA535148 Hs. 255277 ESTs 2.07 101182 L19711 Hs. 76111 dystroglycan 1 (dystrophin-associated gl 2.07 131111 R33245 Hs. 23076 ESTs; Weakly similar to putative [C.eleg 2.07 112441 R63388 Hs. 28412 ESTs 2.06 117796 N48571 Hs. 46689 EST 2.06 116099 AA456309 Hs. 58831 regulator of Fas-induced apoptosis 2.06 125559 AA307550 Hs. 119571 collagen; type III; alpha 1 (Ehlers-Danl 2.06 135271 AA397763 Hs. 97562 ESTs 2.06 106083 AA418545 Hs. 31659 thyroid hormone receptor-associated prot 2.06 133419 U67369 Hs. 73172 growth factor independent 1 2.06 127816 AA743646 Hs. 120604 ESTs 2.06 127502 AA614422 Hs. 183502 ESTs 2.06 129371 M10321 Hs. 110802 von Willebrand factor 2.06 108417 AA075716 zm89e5.s1 Stratagene ovarian cancer (#93 2.06 CLUSTERIN PRECURSOR (HUMAN);, mRNA sequ 102837 U94585 Hs. 13495 requiem; apoptosis response zinc finger 2.06 124226 H62396 Hs. 190266 ESTs 2.06 102254 U28131 Human HMGI-C chimeric transcript mRNA, p 2.06 128472 X87212 Hs. 10029 cathepsin C 2.06 107545 Z82022 Hs. 26433 dolichyl-phosphate (UDP-N-acetylglucosam 2.06 135311 M36089 Hs. 98493 X-ray repair complementing defective rep 2.06 121727 AA420973 Hs. 104234 ESTs 2.06 131846 U02619 Hs. 331 general transcription factor IIIC; polyp 2.06 120415 AA235810 Hs. 182522 ESTs 2.06 110529 H57686 Hs. 37486 ESTs 2.06 104996 AA112307 Hs. 105894 Homo sapiens mRNA; cDNA DKFZp434G231 (fr 2.06 110351 H41222 Hs. 196459 ESTs 2.06 131261 AA223746 Hs. 171776 inositol(myo)-1(or 4)-monophosphatase 1 2.06 110585 H62223 Hs. 133526 ESTs; Weakly similar to !!!! ALU SUBFAMI 2.06 129420 AA234259 Hs. 99816 ESTs 2.06 103796 AA112595 Hs. 31146 Human DNA sequence from clone 1042K10 on 2.06 lyase (EC 4.3.2.2; Adenylosuccinase; AS 3). Contains ESTs; STSs; GS 119782 W72982 Hs. 58262 ESTs 2.06 108641 AA112059 ATP synthase; H+ transporting; mitochond 2.06 134875 U66672 Hs. 180513 ATP-binding cassette; sub-family A (ABC1 2.06 106832 AA482015 Hs. 30114 ESTs; Highly similar to C8 [H. sapiens] 2.06 109403 AA224413 Hs. 86937 ESTs 2.06 115485 AA287667 Hs. 188804 ESTs 2.06 102923 X12517 Hs. 1063 small nuclear ribonucleoprotein polypept 2.06 123320 AA496792 Hs. 139572 EST 2.05 111901 R39066 Hs. 17638 ESTs 2.05 106558 AA455111 Hs. 182447 heterogeneous nuclear ribonucleoprotein 2.05 126885 AA293052 Hs. 10101 ESTs; Weakly similar to coded for by C. 2.05 113429 T85190 Hs. 179808 ESTs 2.05 102270 U30255 Hs. 75888 phosphogluconate dehydrogenase 2.05 103204 X72475 Hs. 192989 H. sapiens mRNA for rearranged Ig kappa I 2.05 106666 AA461072 Hs. 37916 ESTs 2.05 100947 HG907-HT907 Mg44 2.05 102578 U60666 Hs. 57693 testis specific leucine rich repeat prot 2.05 105827 AA398255 Hs. 31520 ESTs 2.05 122324 AA442830 Hs. 98921 EST 2.05 101025 J04823 Hs. 81097 cytochrome c oxidase subunit VIII 2.05 115861 AA431768 Hs. 90259 ESTs; Weakly similar to alpha 1 [H.sapie 2.05 108081 AA045306 Hs. 42996 ESTs 2.05 133994 X74929 Hs. 242463 keratin 8 2.05 119131 R46700 Hs. 129692 ESTs; Moderately similar to !!!! ALU SUB 2.05 129793 AA300151 Hs. 126857 ESTs 2.05 101653 M60284 Hs. 161305 tachykinin receptor 2 2.05 120300 AA191648 Hs. 131476 ESTs 2.05 106519 AA453415 Hs. 8763 Hu DNA sequence from clone 889N15 on chr 2.05 Thymocyte Marker CTX; the possibly alte 114291 Z40690 Hs. 123666 Homo sapiens mRNA full length insert cDN 2.05 105747 AA293719 Hs. 30251 ESTs; Weakly similar to GLUCOSE-6-PHOSPH 2.04 125325 AA332944 Hs. 8402 adenylate cyclase 3 2.04 119978 W88623 Hs. 59190 EST 2.04 102449 U48231 Hs. 46348 bradykinin receptor B1 2.04 101454 M21812 Hs. 50889 myosin light chain 2 2.04 116086 AA455904 Hs. 86023 ESTs 2.04 102297 U32674 Hs. 198252 G protein-coupled receptor 9 2.04 130889 D57622 Hs. 20985 sin3-associated polypeptide; 30 kD 2.04 100196 D21853 Hs. 79768 KIAA0111 gene product 2.04 120967 AA398111 Hs. 97503 ESTs 2.04 105735 AA293096 Hs. 32417 ESTs 2.04 135031 R41604 Hs. 9344 ESTs; Weakly similar to !!!! ALU SUBFAMI 2.04 104882 AA052954 Hs. 29546 ESTs 2.04 132619 AA404565 Hs. 53447 ESTs; Moderately similar to kinesin ligh 2.04 127993 AA847856 Hs. 124565 ESTs 2.04 116441 AA620299 Hs. 91696 ESTs 2.04 102272 U30610 Hs. 41682 killer cell lectin-like receptor subfami 2.04 119566 W38209 Accession not listed in Genbank 2.04 116622 D81171 Hs. 45208 ESTs; Weakly similar to collagen type VI 2.04 127182 AA248620 Hs. 166011 catenin (cadherin-associated protein); d 2.04 116870 H67146 Hs. 38564 ESTs 2.04 115448 AA284845 Hs. 165051 ESTs 2.04 127231 AA434584 zw52c03.r1 Soares_total_fetus_Nb2HF8_9w 2.04 103457 X99728 H. sapiens NDUFV3 gene, exon 3 2.04 134737 U00802 Hs. 89434 drebrin 1 2.04 117046 H89505 yu81f4.s1 Soares fetal liver spleen 1NFL 2.04 to contains Alu repetitive element; mR 124579 N68345 Hs. 127179 ESTs; Weakly similar to TERATOCARCINOMA- 2.04 112132 R45970 Hs. 236349 EST 2.04 132281 AA133300 Hs. 43803 leukocyte-associated Ig-like receptor 2 2.03 103668 Z83741 Hs. 248174 H2A histone family; member M 2.03 113501 T89107 Hs. 13262 ESTs 2.03 125021 T70060 Hs. 163918 ESTs 2.03 115754 AA420998 Hs. 178095 ESTs 2.03 123405 AA521370 Hs. 191708 ESTs 2.03 102054 U07695 Hs. 155227 EphB4 2.03 115627 AA401910 Hs. 119175 ESTs; Weakly similar to ZINC FINGER PROT 2.03 129252 AA234663 Hs. 109773 ESTs 2.03 103417 X96849 H. sapiens 5′ mRNA of PECAM-1 molecule 2.03 133721 U11863 Hs. 75741 amiloride binding protein 1 (amine oxida 2.03 114176 Z39059 Hs. 27267 ESTs; Weakly similar to tetraspan TM4SF 2.03 123966 C14068 Hs. 21806 ESTs; Moderately similar to similar to N 2.03 134236 D45371 Hs. 80485 adipose most abundant gene transcript 1 2.03 116381 AA598614 Hs. 65394 ESTs 2.03 103711 AA046737 Hs. 102792 ESTs 2.03 109316 AA206914 Hs. 86322 EST 2.03 123793 AA620343 Hs. 112858 ESTs 2.03 128462 M69238 Hs. 166172 aryl hydrocarbon receptor nuclear transl 2.03 117690 N40467 Hs. 93834 ESTs 2.03 113301 T67452 Hs. 13104 EST 2.03 134563 AA173430 Hs. 85335 Home sapiens mRNA; cDNA DKFZp564D1462 (f 2.03 108316 AA070160 zm69f4.s1 Stratagene neuroepithelium (#9 2.03 135239 AA454599 Hs. 19399 Homo sapiens chromosome 19; fosmid 39554 2.03 120342 AA207105 Hs. 45068 Home sapiens mRNA; cDNA DKFZp434I143 (fr 2.02 103493 Y08976 Hs. 234759 H. sapiens mRNA for FEV protein 2.02 114204 Z39259 Hs. 26096 ESTs 2.02 125425 H62307 Hs. 18575 ESTs; Weakly similar to KIAA0246 [H.sapi 2.02 133027 AA402624 Hs. 63236 synuclein; gamma (breast cancer-specific 2.02 131323 H54036 Hs. 25619 death-associated protein kinase 3 2.02 121515 AA412133 Hs. 104696 ESTs 2.02 129780 AA291526 Hs. 124699 ESTs 2.02 131292 AF005039 Hs. 200600 secretory carrier membrane protein 3 2.02 132973 AA035446 Hs. 214361 ESTs 2.02 103727 AA059415 Hs. 6289 growth factor receptor-bound protein 2 2.02 113174 T54659 Hs. 9779 ESTs 2.02 120964 AA398085 Hs. 142390 ESTs 2.02 134303 AA457242 Hs. 8141 etoposide-induced mRNA 2.02 128118 T81623 Hs. 21765 hypothetical protein of unknown functio 2.02 121087 AA398751 Hs. 97304 ESTs 2.02 102806 U90306 Human iroquois-class homeodomain protein 2.02 103195 X70940 Hs. 2642 eukaryotic translation elongation factor 2.02 126767 C17148 C17148 Clontech human aorta polyA+ mRNA 2.02 105179 AA189083 Hs. 21974 ESTs; Moderately similar to mBOCT [M.mus 2.02 116797 H40486 yn87a08.s1 Soares adult brain N2b5HB55Y 2.02 3′ similar to contains Alu repetitive e 133268 AA099404 Hs. 69307 ESTs 2.02 123951 AA621721 Hs. 231130 EST 2.02 115463 AA286819 Hs. 69485 ESTs; Weakly similar to similar to other 2.02 110603 H65776 Hs. 222403 ESTs 2.02 101234 L29277 Hs. 142258 signal transducer and activator of trans 2.02 121208 AA400470 Hs. 97805 ESTs 2.02 122598 AA453465 Hs. 99329 ESTs 2.02 110668 H84882 Hs. 33791 ESTs; Weakly similar to K: Cl cotransport 2.02 117137 H96670 Hs. 42221 ESTs 2.02 119389 T88826 Hs. 90973 ESTs 2.01 102940 X13956 Hs. 24998 Human 12S RNA induced by poly(rl); poly( 2.01 100748 HG3517-HT3711 Alpha-1-Antitrypsin, 5′ End 2.01 103012 X52638 Hs. 739 6-phosphofructo-2-kinase/fructose-2; 6-bi 2.01 132755 AA609201 Hs. 182635 ESTs 2.01 130842 H39589 Hs. 20159 ESTs; Highly similar to CGI-92 protein [ 2.01 133599 M64788 Hs. 75151 RAP1; GTPase activating protein 1 2.01 117250 N21081 Hs. 15299 HMBA-inducible 2.01 115124 AA256666 Hs. 39156 ESTs 2.01 128155 AA926843 Hs. 143302 ESTs 2.01 130574 AA379087 Hs. 16178 apoptosis antagonizing transcription fac 2.01 132601 R78838 Hs. 54943 fracture callus 1 (rat) homolog 2.01 117428 N27366 Hs. 43933 EST 2.01 121108 AA399053 Hs. 97529 EST 2.01 130518 X69550 Hs. 159161 Rho GDP dissociation inhibitor (GDI) alp 2.01 110606 H66049 Hs. 19085 ESTs; Weakly similar to putative p150 [H 2.01 120606 AA282956 zt15h4.s1 NCI_CGAP_GCB1 Homo sapiens cDN SW: CADR_MOUSE P3938 RETINAL-CADHERIN PR 2.01 130070 T47969 Hs. 194660 ceroid-lipofuscinosis; neuronal 3; juven 2.01 130331 Z80783 Hs. 239884 H2B histone family; member L 2.01 109599 F02602 Hs. 6749 ESTs 2.01 131749 W78211 Hs. 31547 ESTs; Highly similar to NADH: ubiquinone 2.01 129463 AA376905 Hs. 111742 ESTs; Weakly similar to !!!! ALU SUBFAMI 2.01 114880 AA235698 Hs. 65862 ESTs 2.01 114745 AA135523 Hs. 139064 EST 2.01 115637 AA402727 Hs. 76925 ESTs; Highly similar to R31167_2; partia 2.01 109043 AA159605 Hs. 72580 ESTs 2.01 128901 Z41411 Hs. 107040 ESTs 2.01 124427 N36812 Hs. 178663 ESTs 2 100673 HG3033-HT3194 Spliceosomal Protein Sap 62 2 108436 AA078801 zm94a9.s1 Stratagene colon HT29 (#937221 2 123764 AA610019 Hs. 112654 ESTs 2 129343 N70791 Hs. 180060 ESTs 2 122794 AA460254 Hs. 105043 EST 2 128688 AA161469 Hs. 103755 receptor-interacting serine-threonine ki 2 115592 AA399543 Hs. 48026 ESTs 2 111693 R22007 Hs. 23321 EST 2 113353 T79186 Hs. 14468 ESTs 2

[0344] TABLE 18 B survivor vs Mets - Up in Mets Pkey Ex Accn UniG ID Complete Title Ratio BS/Met 106024 AA412059 Hs. 111742 ESTs; Weakly similar to !!!! ALU SUBFAMI 0.17 110930 N48603 Hs. 14947 ESTs 0.18 105772 AA347973 Hs. 221132 ESTs 0.2 133271 Z48633 Hs. 6940 H. sapiens mRNA for retrotransposon 0.2 107109 AA609943 Hs. 32793 ESTs 0.24 109593 F02506 Hs. 159591 thyroid hormone receptor interactor 8 0.24 123016 AA480103 Hs. 111730 ESTs; Weakly similar to alternatively sp 0.25 100739 HG3484-HT3678 Protein Kinase (Gb: M59287) 0.25 130252 U92014 Hs. 153527 Human clone 121711 defective mariner tra 0.26 105149 AA169253 Hs. 8958 ESTs 0.26 115412 AA283804 Hs. 193552 ESTs 0.27 105952 AA405263 Hs. 181400 ESTs 0.28 106596 AA456981 Hs. 35349 ESTs 0.28 120249 AA167567 Hs. 133325 ESTs 0.28 111676 R19414 Hs. 166459 ESTs 0.29 111161 N66767 Hs. 124145 ESTs 0.29 109364 AA215379 Hs. 50418 ESTs 0.29 132316 U28831 Human protein immuno-reactive with anti- 0.3 104030 AA363131 Hs. 222992 ESTs; Weakly similar to TRANSFORMATION-S 0.3 109825 F13663 Hs. 16798 ESTs 0.3 111110 N63165 Hs. 23618 ESTs 0.31 135315 W90583 Hs. 9853 ESTs 0.32 104792 AA029288 Hs. 29147 ESTs; Highly similar to ZINC FINGER PROT 0.33 123562 AA608893 Hs. 190065 ESTs 0.33 116079 AA455286 Hs. 54982 ESTs; Weakly similar to !!!! ALU SUBFAMI 0.33 110671 H87770 Hs. 153800 ESTs 0.33 108819 AA130986 Hs. 193253 ESTs 0.34 115558 AA393806 Hs. 1010 regulator of mitotic spindle assembly 1 0.34 104781 AA026617 Hs. 21610 ESTs; Highly similar to BAI1-associated 0.34 111236 N69324 Hs. 12526 Homo sapiens clone 23903 mRNA sequence 0.34 113341 T77866 Hs. 189703 ESTs 0.35 125371 AI084676 Hs. 133266 ESTs; Moderately similar to Sqv-7-like p 0.35 115890 AA435853 Hs. 44114 ESTs; Weakly similar to CGI-73 protein [ 0.35 113571 T91116 Hs. 15713 ESTs 0.35 121683 AA417911 Hs. 175663 ESTs 0.35 105489 AA256157 Hs. 24115 ESTs 0.35 116320 AA490866 Hs. 39429 ESTs 0.36 111917 R39882 Hs. 21397 ESTs 0.36 127568 T53722 ya91c06.r3 Stratagene placenta (#937225) 0.36 123541 AA608794 Hs. 112592 ESTs 0.36 123131 AA487207 Hs. 193272 ESTs 0.36 125069 T86914 Hs. 194485 ESTs 0.36 114757 AA136725 Hs. 161990 ESTs 0.37 132778 AA446695 Hs. 5671 Homo sapiens clone 23926 mRNA sequence 0.37 123132 AA487233 Hs. 106711 eukaryotic translation initiation factor 0.37 134029 AA378597 Hs. 143601 ESTs; Moderately similar to 67A9.b [D.me 0.37 126956 AI434405 Hs. 171957 triple functional domain (PTPRF interact 0.38 106869 AA487563 Hs. 188813 ESTs 0.38 107818 AA020957 Hs. 167948 ESTs 0.38 129974 K00629 Hs. 199300 Human kpni repeat mma (cdna clone pcd-k 0.38 129477 D49728 Hs. 1119 nuclear receptor subfamily 4; group A; m 0.38 119369 T79020 Hs. 245915 ESTs; Weakly similar to kinase-related p 0.39 114021 W91995 Hs. 16145 ESTs 0.39 122024 AA431296 Hs. 139433 EST 0.39 130014 N50959 Hs. 143102 amine oxidase; copper containing 2 (reti 0.39 110163 H19326 Hs. 22073 ESTs; Highly similar to J KAPPA-RECOMBIN 0.39 104641 AA004652 Hs. 18564 ESTs 0.39 124777 R41933 Hs. 140237 ESTs 0.39 125382 AA713494 Hs. 194660 ceroid-lipofuscinosis; neuronal 3; juven 0.4 120406 AA234999 Hs. 111279 ESTs; Weakly similar to unnamed protein 0.4 132734 R23653 Hs. 164250 ESTs 0.4 117001 H84719 Hs. 40721 EST 0.4 120905 AA371602 Hs. 182930 ESTs; Highly similar to PHOSPHATIDYLINOS 0.4 125488 AA355158 Hs. 41181 Homo sapiens mRNA; cDNA DKFZp727C191 (fr 0.4 121989 AA430044 Hs. 193784 Homo sapiens mRNA; cDNA DKFZp586K1922 (f 0.4 127921 AA806616 Hs. 209523 ESTs 0.4 119830 W74700 Hs. 53478 ESTs 0.41 106292 AA435571 Hs. 148560 ESTs 0.41 102762 U82303 Hs. 123080 Homo sapiens unknown protein mRNA; parti 0.41 113518 T89731 ye11f06.s1 Stratagene lung (#937210) H.s to contains Alu repetitive element;cont 0.41 100635 HG2724-HT2820 Oncogene Tls/Chop, Fusion Activated 0.41 113319 T70356 Hs. 193141 ESTs; Weakly similar to coding sequence 0.41 121319 AA402935 Hs. 194242 ESTs; Weakly similar to !!!! ALU CLASS B 0.42 111818 R34382 Hs. 24779 ESTs 0.42 104883 AA052959 Hs. 177409 ESTs; Highly similar to dJ1119D9.2 [H.sa 0.42 129258 W95592 Hs. 251946 ESTs; Moderately similar to POLYADENYLAT 0.42 130576 T86475 Hs. 16193 Homo sapiens mRNA; cDNA DKFZp586B211 (fr 0.43 106354 AA443271 Hs. 26764 KIAA0546 protein 0.43 108841 AA132524 Hs. 70614 ESTs 0.43 113922 W80741 Hs. 37890 ESTs 0.43 120997 AA398285 Hs. 97598 EST 0.43 108158 AA054597 Hs. 221935 ESTs 0.43 124516 N58185 Hs. 131830 ESTs 0.43 114477 AA032013 Hs. 144260 EST 0.43 104290 C16652 Hs. 107205 Homo sapiens mRNA; cDNA DKFZp434L2221 (f 0.43 126700 AI318412 Hs. 108258 actin binding protein; macrophin (microf 0.44 110887 N38770 Hs. 4283 ESTs 0.44 116141 AA460420 Hs. 44949 ESTs 0.44 110689 H93046 Hs. 15571 ESTs 0.44 115314 AA280583 Hs. 256501 ESTs 0.44 110904 N39453 Hs. 27371 Homo sapiens mRNA; cDNA DKFZp566J123 (fr 0.44 109482 AA233375 Hs. 78085 ESTs 0.44 102284 U31449 Hs. 11881 transmembrane 4 superfamily member 4 0.44 118654 N70582 Hs. 49892 ESTs 0.44 115334 AA281244 Hs. 65300 ESTs 0.44 113149 T51588 ESTs; Moderately similar to !!!! ALU SUB 0.44 113721 T97931 Hs. 18190 EST 0.44 111299 N73808 Hs. 24936 ESTs 0.44 103778 AA094107 Hs. 7187 ESTs; Weakly similar to similar to glyco 0.44 113204 T57865 Hs. 10310 EST 0.44 100315 D50857 Hs. 82295 dedicator of cyto-kinesis 1 0.44 115254 AA279024 Hs. 194437 ESTs 0.44 125500 H46104 Hs. 244624 ESTs 0.44 117387 N26011 Hs. 53810 ESTs 0.45 135113 W42450 Hs. 206833 ESTs 0.45 124517 N58204 Hs. 199945 ESTs 0.45 120379 AA227849 Hs. 238380 Human endogenous retroviral protease mRN 0.45 119205 R91954 Hs. 153699 ESTs 0.45 128266 T70341 Hs. 131897 ESTs 0.45 104106 AA422123 Hs. 42457 ESTs 0.45 115864 AA432080 Hs. 81200 ESTs 0.45 113771 W02695 Hs. 18714 ESTs 0.45 126515 AI124649 Hs. 252708 Homo sapiens mRNA; cDNA DKFZp586O031 (fr 0.45 127823 AA524806 Hs. 78869 transcription elongation factor A (SII); 0.45 116665 F04405 Hs. 223654 EST 0.45 106355 AA443272 Hs. 27836 ESTs 0.45 132693 AA621429 Hs. 55075 KIAA0410 gene product 0.45 107388 W01587 Hs. 173319 ESTs 0.45 110688 H93021 Hs. 182937 peptidylprolyl isomerase A (cyclophilin 0.46 116893 H69569 Hs. 191316 EST 0.46 105375 AA236542 Hs. 9512 ESTs; Moderately similar to !!!! ALU SUB 0.46 115601 AA400277 Hs. 48849 ESTs 0.46 106896 AA489707 Hs. 29896 ESTs; Weakly similar to proline-rich pro 0.46 111770 R27975 Hs. 187469 ESTs 0.46 115663 AA405838 Hs. 40507 ESTs 0.46 131404 AA504744 Hs. 26461 ESTs; Weakly similar to gc-rich sequence 0.46 108622 AA101828 Hs. 189956 ESTs 0.46 128286 AI025771 Hs. 144090 ESTs 0.46 105760 AA338960 Hs. 28170 ESTs 0.46 100020 AFFX control: BioB-3 0.46 105209 AA205072 Hs. 227743 KIAA0980 protein 0.47 111975 R41724 Hs. 149566 ESTs 0.47 114688 AA121403 Hs. 144331 ESTs 0.47 116994 H83918 Hs. 40528 ESTs 0.47 118401 N64762 Hs. 49053 EST 0.47 110997 N52540 Hs. 74316 desmoplakin (DPI; DPII) 0.47 123791 AA620331 Hs. 245351 EST 0.47 109858 H02266 Hs. 167451 ESTs 0.47 115470 AA287122 Hs. 48391 ESTs 0.47 130606 AA402109 Hs. 16593 ESTs 0.47 116067 AA454827 Hs. 124823 ESTs 0.47 125881 AA775807 Hs. 150741 2′;3′-cyclic nucleotide 3′ phosphodieste 0.47 124028 F04112 Hs. 177178 ESTs 0.47 108995 AA155574 Hs. 172702 ESTs 0.47 125102 T95105 Hs. 173772 ESTs 0.47 110421 H48462 Hs. 36093 ESTs; Weakly similar to reverse transcri 0.47 105658 AA282914 Hs. 10176 ESTs 0.47 129046 AA195678 Hs. 108258 actin binding protein; macrophin (microf 0.47 113639 T95128 Hs. 17529 ESTs 0.48 132575 AA045365 Hs. 5188 ESTs; Weakly similar to 60S RIBOSOMAL PR 0.48 132592 AA129390 Hs. 5285 ESTs 0.48 107619 AA004955 Hs. 60015 ESTs 0.48 118664 N70907 Hs. 230619 EST 0.48 127612 AA917801 Hs. 116076 ESTs 0.48 112319 R55615 Hs. 26432 ESTs; Weakly similar to finger protein H 0.48 113635 T95087 Hs. 15543 ESTs 0.48 119344 T62969 Hs. 193348 ESTs 0.48 121080 AA398720 Hs. 177953 ESTs 0.48 133686 X83378 Hs. 211614 chloride channel 6 0.48 130395 R54534 Hs. 87889 helicase-moi 0.49 127530 AA563806 Hs. 145728 ESTs 0.49 132971 AA033951 Hs. 61700 ESTs 0.49 127132 AA721156 Hs. 190440 ESTs 0.49 129980 T72661 Hs. 13969 ESTs 0.49 105323 AA234112 Hs. 29075 ESTs 0.49 114439 AA018937 Hs. 128629 ESTs 0.49 107632 AA007242 Hs. 60179 EST 0.49 130952 AB002296 Hs. 21560 Human mRNA for KIAA0298 gene; complete c 0.49 127595 AA927308 Hs. 130464 ESTs 0.49 124276 H83465 Hs. 221934 ESTs 0.49 125935 H30721 Hs. 30172 ESTs 0.49 131275 U45974 Hs. 25156 Human phosphatidylinositol (4;5) bisphos 0.49 131196 C20633 Hs. 24129 ESTs 0.49 125505 AI127843 Hs. 155071 ESTs 0.5 113327 T71776 Hs. 12097 ESTs 0.5 104709 AA017146 Hs. 34579 ESTs; Moderately similar to !!!! ALU SUB 0.5 115772 AA423972 Hs. 8154 ESTs 0.5 118296 N63150 Hs. 48723 ESTs 0.5 131453 C20596 Hs. 26985 KIAA0457 protein 0.5 104734 AA019528 Hs. 32677 ESTs 0.5 119358 T70550 Hs. 193651 ESTs; Weakly similar to alternatively sp 0.5

[0345] TABLE 19 B survivor vs Mets - Up in B survivor Pkey Ex Accn UniG_ID Complete Title Ratio BS/Met 333601 CH22_FGENES.213_4 5.5 325300 CH.11_hs gi|5866908 4.67 333642 CH22_FGENES.231_2 4.64 333591 CH22_FGENES.208_4 4.46 332859 CH22_FGENES.27_2 4.39 304013 AW518573 Hs. 156110 Immunoglobulin kappa variable 1D-8 4.23 333791 CH22_FGENES.274_10 4.18 327641 CH.04_hs gi|5867890 4.03 321172 H49160 Hs. 133472 ESTs 3.9 334125 CH22_FGENES.334_4 3.88 333646 CH22_FGENES.234_2 3.88 326554 CH.19_hs gi|5867308 3.84 333650 CH22_FGENES.238_3 3.82 333647 CH22_FGENES.235_2 3.79 333626 CH22_FGENES.224_2 3.68 314671 AW236550 Hs. 131914 ESTs 3.68 310847 AI420523 Hs. 161282 ESTs 3.67 333657 CH22_FGENES.241_2 3.65 338522 CH22_EM: AC005500.GENSCAN.395-36 3.64 329464 CH.Y_hs gi|6456788 3.6 328868 CH.07_hs gi|6381930 3.6 333637 CH22_FGENES.229_2 3.59 329737 CH.14_p2 gi|6065779 3.5 317828 AI791749 Hs. 128896 ESTs 3.44 330520 M96995 Hs. 6289 growth, factor receptor-bound protein 2 3.44 339271 CH22_BA354I12.GENSCAN.11-2 3.44 314927 AI735482 Hs. 159580 ESTs 3.42 334782 CH22_FGENES.432_7 3.42 313138 AW138842 Hs. 196669 ESTs 3.4 332650 H51596 Hs. 5541 ATPase; Ca++ transporting; ubiquitous 3.38 338648 CH22_EM: AC005500.GENSCAN.460-6 3.38 325677 CH.14_hs gi|5867017 3.34 312639 H50648 Hs. 213221 ESTs; Weakly similar to !!!! ALU SUBFAMI 3.33 326545 CH.19_hs gi|5867307 3.32 318354 R44616 Hs. 138280 ESTs; Moderately similar to !!!! ALU SUB 3.3 308385 AI625428 EST singleton (not in UniGene) with exon 3.26 328569 CH.07_hs gi|6004480 3.26 328582 CH.07_hs gi|6006033 3.24 310975 AI492857 Hs. 170940 ESTs 3.24 336883 CH22_FGENES.322-2 3.21 324425 AW236939 Hs. 172154 ESTs 3.2 337870 CH22_EM: AC005500.GENSCAN.48-3 3.19 306624 AI001043 EST singleton (not in UniGene) with exon 3.17 319091 Z45264 EST cluster (not in UniGene) 3.16 335247 CH22_FGENES.516_8 3.12 324945 AA088768 EST cluster (not in UniGene) 3.1 319468 R06504 EST cluster (not in UniGene) 3.09 301635 AI590720 Hs. 192662 ESTs; Weakly similar to ZINC FINGER PROT 3.08 321215 AW378128 Hs. 120243 ESTs; Weakly similar to CGI-56 protein [ 3.04 328507 CH.07_hs gi|5868473 3.03 330266 CH.05_p2 gi|6671885 3.02 326249 CH.17_hs gi|5867263 3.01 325649 CH.14_hs gi|6588011 2.99 304575 AA496437 EST singleton (not in UniGene) with exon 2.98 304559 AA488050 EST singleton (not in UniGene) with exon 2.97 338412 CH22_EM: AC005500.GENSCAN.341-25 2.96 308707 AI769997 EST singleton (not in UniGene) with exon 2.95 313027 N34307 Hs. 184003 ESTs; Weakly similar to !!!! ALU SUBFAMI 2.95 306590 AI000246 EST singleton (not in UniGene) with exon 2.95 306183 AA922622 EST singleton (not in UniGene) with exon 2.94 308611 AI735372 Hs. 203820 EST; Moderately similar to TRANSLATIONAL 2.94 332454 T63265 Hs. 11186 ESTs; Weakly similar to transformation-r 2.94 330061 CH.17_p2 gi|6721261 2.94 317671 AW138139 Hs. 244598 ESTs 2.93 338705 CH22_EM: AC005500.GENSCAN.480-4 2.93 333737 CH22_FGENES.261_1 2.9 337756 CH22_EM: AC000097.GENSCAN.109-3 2.9 333572 CH22_FGENES.189_1 2.89 335349 CH22_FGENES.539_2 2.89 328835 CH.07_hs gi|5868339 2.89 319886 AA984628 EST cluster (not in UniGene) 2.88 311247 AI655313 Hs. 197692 ESTs 2.87 303887 R72672 Hs. 193484 ESTs; Weakly similar to Similarity with 2.86 337564 CH22_C65E1.GENSCAN.1-7 2.85 333225 CH22_FGENES.107_3 2.84 314938 AA515635 EST cluster (not in UniGene) 2.83 305803 AA846052 EST singleton (not in UniGene) with exon 2.83 305264 AA679505 EST singleton (not in UniGene) with exon 2.83 332646 AA386264 Hs. 5337 isocitrate dehydrogenase 2 (NADP+); mito 2.81 338508 CH22_EM: AC005500.GENSCAN.391-1 2.81 308097 AI475411 EST singleton (not in UniGene) with exon 2.81 301130 AW194167 Hs. 149418 ESTs; Weakly similar to salivary proline 2.8 325571 CH.12_hs gi|6552439 2.8 307054 AI148181 Hs. 176835 EST 2.8 337456 CH22_FGENES.777-2 2.79 317870 AI797066 Hs. 201995 ESTs 2.79 303171 AA065003 Hs. 64179 hypothetical protein 2.78 333717 CH22_FGENES.253_3 2.76 303778 AW505368 EST cluster (not in UniGene) with exon h 2.76 304918 AA602697 EST singleton (not in UniGene) with exon 2.76 319373 R00371 EST cluster (not in UniGene) 2.75 336072 CH22_FGENES.685_4 2.74 306023 AA897764 EST singleton (not in UniGene) with exon 2.74 336127 CH22_FGENES.701_15 2.74 337355 CH22_FGENES.728-1 2.73 337885 CH22_EM: AC005500.GENSCAN.54-3 2.73 308506 AI686791 Hs. 119598 ribosomal protein L3 2.73 300629 AA152119 Hs. 155101 ATP synthase; H+ transporting; mitochond 2.73 333043 CH22_FGENES.70_4 2.72 327736 CH.05_hs gi|5867940 2.72 333007 CH22_FGENES.60_4 2.72 321966 AL122111 EST cluster (not in UniGene) 2.72 323179 AW452576 Hs. 156875 ESTs 2.72 332459 AA609625 Hs. 112933 Homo sapiens Tax interaction protein 40 2.71 326224 CH.17_hs gi|5867230 2.71 329114 CH.X_hs gi|5868650 2.7 333577 CH22_FGENES.196_2 2.69 300413 AW090347 Hs. 243443 ESTs 2.67 304055 R07994 EST singleton (net in UniGene) with exon 2.67 301013 AI935304 Hs. 125262 DKFZP586G1624 protein 2.67 337848 CH22_EM: AC005500.GENSCAN.33-1 2.66 327946 CH.06_hs gi|5868206 2.66 306300 AA937573 EST singleton (not in UniGene) with exon 2.66 331071 R01646 Hs. 200538 ESTs 2.65 304841 AA587541 EST singleton (not in UniGene) with exon 2.65 301321 AI860987 Hs. 189097 ESTs 2.65 311280 AI767957 Hs. 197737 ESTs; Weakly similar to Y38A8.1 gene pro 2.65 338843 CH22_DJ246D7.GENSCAN.8-1 2.64 335720 CH22_FGENES.599_23 2.64 333670 CH22_FGENES.245_4 2.64 313588 AI803591 Hs. 209667 ESTs 2.64 335750 CH22_FGENES.602_4 2.63 333240 CH22_FGENES.111_4 2.63 332721 R70212 Hs. 79630 CD79A antigen (immunoglobulin-associated 2.62 338747 CH22_EM: AC005500.GENSCAN.511-1 2.62 303582 AA377444 EST cluster (not in UniGene) with exon h 2.62 336898 CH22_FGENES.330-1 2.62 325835 CH.16_hs gi|6552452 2.62 301660 F13112 EST cluster (not in UniGene) with exon h 2.61 335968 CH22_FGENES.652_1 2.61 336705 CH22_FGENES.63-2 2.6 309815 AW292760 EST singleton (not in UniGene) with exon 2.6 339220 CH22_FF113D11.GENSCAN.6-15 2.6 308582 AI709056 EST singleton (not in UniGene) with exon 2.6 334260 CH22_FGENES.367_8 2.6 309963 AW449073 EST singleton (not in UniGene) with exon 2.6 300178 AI282665 Hs. 166969 ESTs 2.59 335690 CH22_FGENES.596_5 2.59 308127 AI492187 EST singleton (not in UniGene) with exon 2.59 337835 CH22_EM: AC005500.GENSCAN.22-4 2.58 333251 CH22_FGENES.116_3 2.58 330319 CH.08_p2 gi|5932415 2.58 314490 AI758114 Hs. 197032 ESTs 2.57 305934 AA878815 Hs. 75442 albumin 2.57 329665 CH.14_p2 gi|6272129 2.57 328558 CH.07_hs gi|5868489 2.57 336094 CH22_FGENES.691_3 2.57 307899 AI380270 EST singleton (not in UniGene) with exon 2.57 339312 CH22_BA354|12.GENSCAN.22-10 2.57 336442 CH22_FGENES.827_8 2.57 317894 R60848 EST cluster (not in UniGene) 2.56 330435 HG2689-HT2785 Mucin 5b, Tracheobronchial (Gb: X74955) 2.56 327304 CH.01_hs gi|5867494 2.56 308859 AI830787 EST singleton (not in UniGene) with exon 2.55 302224 AI951549 Hs. 161166 KIAA1094 protein 2.55 304324 AA137045 EST singleton (not in UniGene) with exon 2.54 338090 CH22_EM: AC005500.GENSCAN.176-3 2.53 334797 CH22_FGENES.434_5 2.52 303535 AL043430 EST cluster (not in UniGene) with exon h 2.52 339037 CH22_DA59H18.GENSCAN.26-5 2.52 327846 CH.05_hs gi|6531962 2.52 325271 CH.11_hs gi|5866901 2.52 312385 R42885 Hs. 215555 ESTs 2.51 302816 AI733918 Hs. 204112 ESTs; Weakly similar to alternatively sp 2.51 316941 AW449871 Hs. 124591 ESTs 2.5 300184 AI285912 Hs. 254515 ESTs 2.5 333762 CH22_FGENES.270_2 2.5 317028 AA962623 Hs. 189144 ESTs; Weakly similar to RENAL SODIUM-DEP 2.5 326266 CH.17_hs gi|5867264 2.49 326005 CH.16_hs gi|5867112 2.49 301971 AJ003125 Hs. 120330 a disintegrin-like and metalloprotease ( 2.48 326539 CH.19_hs gi|5867307 2.48 338896 CH22_DJ32I10.GENSCAN.9-4 2.48 306773 AI040750 EST singleton (not in UniGene) with exon 2.47 336279 CH22_FGENES.763_3 2.47 321017 AL050345 Hs. 227637 hypothetical protein 2.47 306090 AA908609 EST singleton (not in UniGene) with exon 2.47 333216 CH22_FGENES.104_8 2.46 338593 CH22_EM: AC005500.GENSCAN.435-2 2.46 333587 CH22_FGENES.205_2 2.46 300396 AW295466 Hs. 232051 ESTs 2.45 304693 AA554263 EST singleton (not in UniGene) with exon 2.45 338934 CH22_DJ32I10.GENSCAN.18-2 2.45 325751 CH.14_hs gi|6682474 2.45 334137 CH22_FGENES.337_1 2.45 333581 CH22_FGENES.200_1 2.45 302083 AI422807 Hs. 134012 C1q-related factor 2.44 307318 AI208577 EST singleton (not in UniGene) with exon 2.44 302181 AW374284 Hs. 157732 Homo sapiens chromosome 19; cosmid R2689 2.44 337425 CH22_FGENES.761-1 2.44 336227 CH22_FGENES.730_2 2.44 314657 AI015953 Hs. 125265 ESTs 2.44 338529 CH22_EM: AC005500.GENSCAN.398-10 2.44 333680 CH22_FGENES.247_7 2.43 324834 AJ003258 Hs. 250891 ESTs 2.43 305093 AA642917 EST singleton (not in UniGene) with exon 2.43 335787 CH22_FGENES.611_3 2.43 311704 AI655206 Hs. 121512 ESTs; Moderately similar to kinesin like 2.43 329382 CH.X_hs gi|5868868 2.42 334785 CH22_FGENES.432_10 2.42 330130 CH.21_p2 gi|6002196 2.42 327206 CH.01_hs gi|5867447 2.41 319235 F11330 Hs. 177633 ESTs 2.41 334691 CH22_FGENES.420_4 2.4 327610 CH.04_hs gi|5867868 2.4 327646 CH.04_hs gi|5867894 2.4 337093 CH22_FGENES.465-18 2.4 335081 CH22_FGENES.488_4 2.4 333576 CH22_FGENES.193_2 2.4 337604 CH22_C20H12.GENSCAN.16-5 2.4 329879 CH.15_p2 gi|6466518 2.4 328444 CH.07_hs gi|5868420 2.39 335700 CH22_FGENES.598.1 2.39 331255 Z41009 Hs. 21446 ESTs; Weakly similar to HYPOTHETICAL PRO 2.39 327927 CH.06_hs gi|5868173 2.39 334354 CH22_FGENES.377_1 2.39 308517 AI689279 EST singleton (not in UniGene) with exon 2.39 303669 AW499648 Hs. 233750 copine V 2.39 333648 CH22_FGENES.237_2 2.38 318318 AI653893 Hs. 174463 ESTs; Weakly similar to alpha3b subunit 2.38 338336 CH22_EM: AC005500.GENSCAN.310-8 2.38 304125 H40976 EST singleton (not in UniGene) with exon 2.38 304983 AA617786 EST singleton (not in UniGene) with exon 2.38 334935 CH22_FGENES.464_3 2.38 314326 AW170057 Hs. 133179 ESTs 2.38 330406 D49490 Hs. 76901 for protein disulfide isomerase-related 2.38 307646 AI302236 EST singleton (not in UniGene) with exon 2.38 338911 CH22_DJ32I10.GENSCAN.11-3 2.38 319952 T79532 Hs. 225725 ESTs; Moderately similar to CGI-101 prot 2.37 336878 CH22_FGENES.318-5 2.37 338140 CH22_EM: AC005500.GENSCAN.203-6 2.37 300564 AI383878 Hs. 225588 ESTs 2.37 304635 AA523976 EST singleton (not in UniGene) with exon 2.37 334091 CH22_FGENES.327_47 2.37 336328 CH22_FGENES.812_7 2.37 325310 CH.11_hs gi|5866864 2.37 338043 CH22_EM: AC005500.GENSCAN.153-2 2.37 307090 AI161024 EST singleton (not in UniGene) with exon 2.37 335768 CH22_FGENES.607_2 2.37 334969 CH22_FGENES.466_2 2.37 333640 CH22_FGENES.230_2 2.36 330002 CH.16_p2 gi|6623963 2.36 338829 CH22-DJ246D7.GENSCAN.5-12 2.36 323808 AW250114 EST cluster (not in UniGene) 2.36 327755 CH.05_hs gi|5867955 2.35 306426 AA975039 EST singleton (not in UniGene) with exon 2.35 336481 CH22_FGENES.830_1 2.35 335163 CH22_FGENES.502_7 2.35 322012 AL137357 EST cluster (not in UniGene) 2.35 337345 CH22_FGENES.723-1 2.35 334625 CH22_FGENES.414_3 2.35 320957 AI878933 EST cluster (not in UniGene) 2.35 334915 CH22_FGENES.457_4 2.35 336295 CH22_FGENES.787_1 2.35 321556 N46402 Hs. 14570 ESTs 2.35 338491 CH22_EM: AC005500.GENSCAN.385-2 2.35 335517 CH22_FGENES.571_34 2.34 330639 X90872 Hs. 75854 SULT1C sulfotransferase 2.34 310383 AI263102 Hs. 145596 ESTs 2.34 331526 N49967 Hs. 46624 ESTs 2.34 334396 CH22_FGENES.381_2 2.34 332993 CH22_FGENES.57_2 2.34 327487 CH.02_hs gi|5867785 2.34 335920 CH22_FGENES.636_16 2.33 336463 CH22_FGENES.829_22 2.33 319000 Z44318 EST cluster (not in UniGene) 2.33 332992 CH22_FGENES.57_1 2.33 332920 CH22_FGENES.37_6 2.33 337590 CH22_C20H12.GENSCAN.6-5 2.33 327059 CH.21_hs gi|6531965 2.33 334399 CH22_FGENES.382_5 2.33 300982 AA837754 EST cluster (not in UniGene) with, exon h 2.32 327430 CH.02_hs gi|5867754 2.32 326808 CH.20_hs gi|6682504 2.32 309324 AW015373 EST singleton (not in UniGene) with exon 2.32 329779 CH.14_p2 gi|6002090 2.32 330492 M25809 Hs. 64173 ATPase; H+ transporting; lysosomal (vacu 2.31 330080 CH.19_p2 gi|6015314 2.31 334342 CH22_FGENES.375_20 2.31 336306 CH22_FGENES.793_5 2.31 336400 CH22_FGENES.823_15 2.31 323735 AA323714 EST cluster (not in UniGene) 2.31 334496 CH22_FGENES.397_12 2.31 336075 CH22_FGENES.687_1 2.31 335566 CH22_FGENES.580_1 2.31 337657 CH22_EM: AC000097.GENSCAN.32-9 2.31 327816 CH.05_hs gi|5867968 2.3 308465 AI672480 EST singleton (not in UniGene) with exon 2.3 330112 CH.19_p2 gi|6015238 2.3 304465 AA421948 EST singleton (not in UniGene) with exon 2.3 308449 AI660854 EST singleton (not in UniGene) with exon 2.3 328171 CH.06_hs gi|5868071 2.3 328271 CH.06_hs gi|6552415 2.3 328803 CH.07_hs gi|6004475 2.3 330063 CH.19_p2 gi|6165044 2.29 312281 H11643 EST cluster (not in UniGene) 2.29 328974 CH.09_hs gi|5868520 2.29 333859 CH22_FGENES.290_18 2.29 326253 CH.17_hs gi|5867263 2.29 325703 CH.14_hs gi|5867028 2.29 338925 CH22_DJ32I10.GENSCAN.14-3 2.29 328552 CH.07_hs gi|5868489 2.29 337244 CH22_FGENES.646-8 2.29 314770 AI732722 Hs. 187694 ESTs 2.29 324560 AW502208 EST cluster (not in UniGene) 2.29 310603 AW376860 Hs. 156398 ESTs 2.29 337363 CH22_FGENES.733-2 2.29 308015 AI440174 Hs. 228907 EST; Weakly similar to GUANINE NUCLEOTID 2.28 309206 AI961962 EST singleton (not in UniGene) with exon 2.28 337455 CH22_FGENES.777-1 2.28 327605 CH.03_hs gi|6004463 2.28 301611 W22172 Hs. 59038 ESTs 2.28 317222 AI206964 Hs. 130051 ESTs 2.28 338278 CH22_EM: AC005500.GENSCAN.290-3 2.28 337291 CH22_FGENES.673-2 2.27 337913 CH22_EM: AC005500.GENSCAN.59-10 2.27 306406 AA971973 EST singleton (not in UniGene) with exon 2.27 332947 CH22_FGENES.47_10 2.27 321763 W01148 EST cluster (not in UniGene) 2.27 304424 AA293494 EST singleton (not in UniGene) with exon 2.27 303782 T64737 EST cluster (not in UniGene) with exon h 2.27 326943 CH.21_hs gi|6004446 2.27 324977 R14439 Hs. 209194 ESTs 2.27 325480 CH.12_hs gi|5866957 2.27 327743 CH.05_hs gi|5867944 2.27 333221 CH22_FGENES.105_1 2.26 336498 CH22_FGENES.833_3 2.26 321583 H84421 EST cluster (not in UniGene) 2.26 334191 CH22_FGENES.352_6 2.26 327089 CH.21_hs gi|6531965 2.26 310001 F18939 Hs. 153827 ESTs 2.26 304056 R08577 EST singleton (not in UniGene) with exon 2.25 324700 AW504745 Hs. 103913 ESTs; Moderately similar to !!!! ALU SUB 2.25 330637 X86371 Hs. 95659 lethal giant larvae (Drosophila) homolog 2.25 307642 AI302103 EST singleton (not in UniGene) with exon 2.25 336985 CH22_FGENES.402-6 2.25 334425 CH22_FGENES.384_13 2.25 321216 AI078042 Hs. 126691 ESTs 2.25 315785 AW205946 Hs. 150319 ESTs 2.25 305809 AA853998 Hs. 124580 EST 2.25 331334 AA284858 Hs. 89134 ESTs 2.25 317131 AI991125 Hs. 189109 ESTs 2.25 334216 CH22_FGENES.358_1 2.24 330330 CH.08_p2 gi|5670267 2.24 326923 CH.21_hs gi|6456782 2.24 333774 CH22_FGENES.272_5 2.24 324311 AA443061 Hs. 202520 ESTs 2.24 338551 CH22_EM: AC005500.GENSCAN.413-2 2.24 306716 AI024916 Hs. 251354 ESTs 2.24 337689 CH22_EM: AC000097.GENSCAN.77-5 2.24 300079 AI192520 Hs. 147178 EST 2.23 334617 CH22_FGENES.411_16 2.23 336890 CH22_FGENES.326-10 2.23 334495 CH22_FGENES.397_10 2.23 327301 CH.01_hs gi|5867493 2.23 337856 CH22_EM: AC005500.GENSCAN.41-3 2.23 307072 AI150424 Hs. 146817 EST 2.23 330515 M85247 H. sapiens dopamine D1A receptor gene, co 2.22 325943 CH.16_hs gi|5867138 2.22 338947 CH22_DJ32I10.GENSCAN.21-4 2.22 317465 AW197361 Hs. 131360 ESTs 2.22 332458 M33493 Hs. 184504 tryptase; alpha 2.22 333195 CH22_FGENES.98_17 2.22 304837 AA587139 EST singleton (not in UniGene) with exon 2.22 307602 AI288843 Hs. 231239 EST 2.22 337078 CH22_FGENES.457-1 2.22 335862 CH22_FGENES.629_7 2.22 301979 L28168 Hs. 121495 potassium voltage-gated channel; lsk-rel 2.22 335668 CH22_FGENES.590_19 2.22 305068 AA639618 EST singleton (not in UniGene) with exon 2.21 329034 CH.X_hs gi|5868561 2.21 318403 AI131241 Hs. 143234 ESTs 2.21 328058 CH.06_hs gi|5902482 2.21 335513 CH22_FGENES.571_28 2.21 330803 AA004699 Hs. 150580 putative translation initiation factor 2.21 331427 H54764 Hs. 237339 EST 2.21 338973 CH22_DJ32I10.GENSCAN.27-6 2.2 336723 CH22_FGENES.85-3 2.2 327290 CH.01_hs gi|5867483 2.2 337240 CH22_FGENES.644-1 2.2 306201 AA926818 EST singleton (not in UniGene) with exon 2.2 303659 AA868464 Hs. 126263 ESTs; Highly similar to FIBRILLARIN [H.s 2.2 334517 CH22_FGENES.399_7 2.2 334189 CH22_FGENES.352_4 2.2 335199 CH22_FGENES.508_8 2.2 333705 CH22_FGENES.250_19 2.2 305794 AA845324 EST singleton (not in UniGene) with exon 2.2 303273 AA316069 EST cluster (not in UniGene) with exon h 2.2 313384 W85694 Hs. 118335 ESTs 2.2 329158 CH.X_hs gi|5868687 2.2 337551 CH22_FGENES.847-8 2.2 328792 CH.07_hs gi|5868309 2.2 303737 AW502711 EST cluster (not in UniGene) with exon h 2.19 324529 AW502466 EST cluster (not in UniGene) 2.19 323103 Z45529 Hs. 92030 ESTs 2.19 333773 CH22_FGENES.272_4 2.19 337906 CH22_EM: AC005500.GENSCAN.56-19 2.19 327129 CH.21_hs gi|6531976 2.19 305710 AA826544 EST singleton (not in UniGene) with exon 2.19 335595 CH22_FGENES.581_34 2.19 323646 AA310926 Hs. 154412 ESTs 2.19 328368 CH.07_hs gi|5868388 2.19 325802 CH.14_hs gi|6552451 2.19 337167 CH22_FGENES.562-27 2.19 305059 AA635756 EST singleton (not in UniGene) with exon 2.18 321445 AW245524 Hs. 121590 ESTs; Weakly similar to ZINC FINGER PROT 2.18 332790 CH22_FGENES.2_4 2.18 336750 CH22_FGENES.128-4 2.18 310999 AI520706 Hs. 171012 ESTs 2.18 329798 CH.14_p2 gi|6523160 2.18 327012 CH.21_hs gi|5867664 2.18 304599 AA506638 EST singleton (not in UniGene) with exon 2.18 335351 CH22_FGENES.539_4 2.18 310661 AI354717 Hs. 223908 ESTs 2.18 332791 CH22_FGENES.3_1 2.17 333022 CH22_FGENES.65_1 2.17 310502 AI458973 Hs. 170422 ESTs 2.17 324963 AA853440 EST cluster (not in UniGene) 2.17 325275 CH.11_hs gi|5866902 2.17 328338 CH.07_hs gi|5868377 2.17 333063 CH22_FGENES.75_6 2.17 308895 AI858423 EST singleton (not in UniGene) with exon 2.17 338685 CH22_EM: AC005500.GENSCAN.472-4 2.16 325655 CH.14_hs gi|5867007 2.16 332420 H49570 Hs. 108074 ESTs; Weakly similar to CEREBELLIN 1 PRE 2.16 337216 CH22_FGENES.613-10 2.16 335660 CH22_FGENES.590_11 2.16 337145 CH22_FGENES.542-2 2.16 335753 CH22_FGENES.604_2 2.16 301766 R02224 EST cluster (not in UniGene) with exon h 2.16 303442 AI953998 Hs. 152510 ESTs; Weakly similar to L-SERINE DEHYDRA 2.16 311009 AI949701 Hs. 210589 ESTs 2.16 307093 AI167606 EST singleton (not in UniGene) with exon 2.16 300262 AI874402 Hs. 170810 ESTs 2.16 337989 CH22_EM: AC005500.GENSCAN.112-7 2.16 326263 CH.17_hs gi|5867264 2.16 319402 W21298 EST cluster (not in UniGene) 2.16 321010 Y17456 Hs. 227150 Homo sapiens LSFR2 gene; last exon 2.16 301706 AI929150 Hs. 241496 ESTs 2.16 307412 AI241753 Hs. 241507 ribosomal protein S6 2.16 335662 CH22_FGENES.590_13 2.15 332480 AA092932 Hs. 12570 tubulin-specific chaperone d 2.15 329273 CH.X_hs gi|5868762 2.15 339383 CH22_BA232E17.GENSCAN.3-20 2.15 332795 CH22_FGENES.5_1 2.15 335227 CH22_FGENES.513_13 2.15 326925 CH.21_hs gi|6456782 2.15 332403 AA424199 Hs. 106529 ESTs; Highly similar to CGI-65 protein [ 2.15 317786 AI859605 Hs. 155686 ESTs 2.15 326582 CH.19_hs gi|5867318 2.15 336494 CH22_FGENES.832_11 2.15 329656 CH.14_p2 gi|6448516 2.15 307581 AI284415 EST singleton (not in UniGene) with exon 2.15 335670 CH22_FGENES.591_2 2.14 332452 AA040369 Hs. 11170 SYT interacting protein 2.14 309387 AW079943 Hs. 156110 Immunoglobulin kappa variable 1D-8 2.14 308427 AI652677 Hs. 195055 EST 2.14 322027 NM_004551 EST cluster (not in UniGene) 2.14 301693 Z45023 EST cluster (not in UniGene) with exon h 2.14 334308 CH22_FGENES.373_11 2.14 301131 AW134518 Hs. 131807 ESTs 2.13 338495 CH22_EM: AC005500.GENSCAN.387-1 2.13 329600 CH.10_p2 gi|3962481 2.13 307980 AI431696 EST singleton (not in UniGene) with exon 2.13 337260 CH22_FGENES.652-15 2.13 304655 AA527887 EST singleton (not in UniGene) with exon 2.13 303141 AF195951 EST cluster (not in UniGene) with exon h 2.13 327957 CH.06_hs gi|5868210 2.13 334317 CH22_FGENES.374_1 2.13 302870 AF011407 EST cluster (not in UniGene) with exon h 2.13 333806 CH22_FGENES.278_2 2.13 329947 CH.16_p2 gi|5540101 2.13 309602 AW182523 EST singleton (not in UniGene) with exon 2.13 322790 AI700273 Hs. 122162 ESTs; Weakly similar to KIAA0557 protein 2.13 337706 CH22_EM: AC000097.GENSCAN.87-11 2.13 306894 AI092731 EST singleton (not in UniGene) with exon 2.13 325530 CH.12_hs gi|6525289 2.12 321087 AL110227 Hs. 241533 Homo sapiens mRNA; cDNA DKFZp434J194 (fr 2.12 309853 AW298169 Hs. 57553 tousled-like kinase 2 2.12 326822 CH.20_hs gi|6117831 2.12 328776 CH.07_hs gi|5868309 2.12 335112 CH22_FGENES.494_20 2.12 334564 CH22_FGENES.405_4 2.12 333455 CH22_FGENES.157_4 2.12 317395 R55044 Hs. 124130 ESTs 2.12 334221 CH22_FGENES.360_1 2.12 331374 AA442134 Hs. 70573 ESTs; Weakly similar to HINT PROTEIN [H. 2.12 304473 AA428343 Hs. 140 immunoglobulin gamma 3 (Gm marker) 2.12 328907 CH.08_hs gi|5868493 2.12 319448 R05539 Hs. 108738 ESTs 2.12 333676 CH22_FGENES.247_3 2.12 324767 AA630931 Hs. 34348 Homo sapiens mRNA; cDNA DKFZp434P0235 (f 2.12 318585 Z43405 EST cluster (not in UniGene) 2.12 331732 AA251192 Hs. 177708 ESTs 2.12 329553 CH.10_p2 gi|3962492 2.12 336910 CH22_FGENES.343-6 2.12 326959 CH.21_hs gi|6469836 2.12 305417 AA725228 EST singleton (not in UniGene) with exon 2.11 301573 AI150328 Hs. 226402 ESTs; Weakly similar to mitochondrial ci 2.11 326935 CH.21_hs gi|6004446 2.11 335176 CH22_FGENES.504_6 2.11 337210 CH22_FGENES.603-5 2.11 311284 AW027025 Hs. 239262 ESTs 2.11 330240 CH.05_p2 gi|6671858 2.11 327463 CH.02_hs gi|6004455 2.11 332938 CH22_FGENES.41_3 2.11 332785 CH22_FGENES.1_1 2.11 301035 AI358105 Hs. 123164 ESTs 2.1 305712 AA826701 EST singleton (not in UniGene) with exon 2.1 318651 AW003150 Hs. 240165 ESTs 2.1 302753 M74299 EST cluster (not in UniGene) with exon h 2.1 334635 CH22_FGENES.417_2 2.1 319447 AA456745 EST cluster (not in UniGene) 2.1 301204 AW008544 Hs. 239994 ESTs 2.1 333950 CH22_FGENES.303_6 2.1 325947 CH.16_hs gi|5867138 2.1 337683 CH22_EM: AC000097.GENSCAN.76-1 2.1 328962 CH.08_hs gi|6456775 2.1 336655 CH22_FGENES.34-3 2.1 336596 CH22_FGENES.163_2 2.1 330486 M13755 Hs. 833 interferon-stimulated protein; 15 kDa 2.1 314356 AA531607 Hs. 125143 ESTs 2.09 314976 AA524725 Hs. 162108 ESTs 2.09 336650 CH22_FGENES.29-6 2.09 339026 CH22_DA59H18.GENSCAN.22-6 2.09 302395 AW297357 Hs. 114606 ESTs 2.09 323280 AI910263 EST cluster (not in UniGene) 2.09 338857 CH22_DJ32I10.GENSCAN.1-1 2.09 335374 CH22_FGENES.543_12 2.09 308766 AI808510 EST singleton (not in UniGene) with exon 2.09 331027 N48584 Hs. 6168 KIAA0703 gene product 2.09 337853 CH22_EM: AC005500.GENSCAN.37-1 2.09 302498 NM_002991 EST cluster (not in UniGene) with exon h 2.09 312607 AI337440 Hs. 169375 ESTs 2.09 314309 Z44049 Hs. 184352 ESTs; Weakly similar to cDNA EST EMBL: D3 2.09 311695 AI142078 Hs. 135562 ESTs 2.09 333280 CH22_FGENES.126_2 2.09 333518 CH22_FGENES.173_3 2.09 337199 CH22_FGENES.583-11 2.09 337819 CH22_EM: AC005500.GENSCAN.13-9 2.08 300546 AA214450 Hs. 250913 ESTs 2.08 322577 AA354452 Hs. 59075 ESTs; Weakly similar to WD40 protein Cia 2.08 336028 CH22_FGENES.672_1 2.08 300238 AI394673 Hs. 254030 ESTs 2.08 307429 AI243573 EST singleton (not in UniGene) with exon 2.08 326444 CH.19_hs gi|5867385 2.08 310641 AI345597 Hs. 254727 ESTs 2.08 337633 CH22_C20H12.GENSCAN.32-1 2.08 336008 CH22_FGENES.668_6 2.08 339030 CH22_DA59H18.GENSCAN.24-1 2.08 333952 CH22_FGENES.303_8 2.08 329149 CH.X_hs gi|5868685 2.08 335192 CH22_FGENES.507_7 2.08 308225 AI557713 Hs. 177592 ribosomal protein; large; P1 2.08 330519 M94172 Hs. 69949 calcium channel; voltage-dependent; L ty 2.08 331809 AA402482 Hs. 97312 ESTs 2.07 324837 AJ003669 Hs. 246171 ESTs 2.07 332608 D00749 Hs. 36972 CD7 antigen (p41) 2.07 327291 CH.01_hs gi|5867483 2.07 315936 AW069807 Hs. 247094 ESTs; Moderately similar to !!!! ALU SUB 2.07 317917 AI143593 Hs. 129419 ESTs 2.07 328674 CH.07_hs gi|5868254 2.07 338654 CH22_EM: AC005500.GENSCAN.460-55 2.07 320828 AJ012590 Hs. 194728 hexose-6-phosphate dehydrogenase (glucos 2.07 337896 CH22_EM: AC005500.GENSCAN.56-3 2.07 335310 CH22_FGENES.532_3 2.07 300076 AW074835 Hs. 145223 ESTs 2.07 303588 AL046182 EST cluster (not in UniGene) with exon h 2.07 328848 CH.07_hs gi|6381921 2.07 318723 C18060 EST cluster (not in UniGene) 2.07 335352 CH22_FGENES.539_5 2.07 339316 CH22_BA354I12.GENSCAN.22-15 2.06 335873 CH22_FGENES.631_1 2.06 335261 CH22_FGENES.520_2 2.06 322032 AL079807 EST cluster (not in UniGene) 2.06 308771 AI809301 EST singleton (not in UniGene) with exon 2.06 310024 AI252661 Hs. 145224 ESTs 2.06 320555 R36212 Hs. 235534 ESTs 2.06 319314 T74062 EST cluster (not in UniGene) 2.06 334642 CH22_FGENES.417_9 2.06 335767 CH22_FGENES.607_1 2.06 336159 CH22_FGENES.707_3 2.06 336358 CH22_FGENES.818_1 2.06 334687 CH22_FGENES.419_12 2.06 339389 CH22_BA232E17.GENSCAN.4-7 2.06 335898 CH22_FGENES.635_6 2.06 328847 CH.07_hs gi|6381920 2.06 313431 W91884 EST cluster (not in UniGene) 2.06 313270 AI374993 Hs. 159611 ESTs 2.06 339211 CH22_FF113D11.GENSCAN.6-6 2.06 333860 CH22_FGENES.290_19 2.06 308952 AI868157 Hs. 224226 EST 2.06 305471 AA743947 EST singleton (not in UniGene) with exon 2.06 300619 AA991438 Hs. 233293 ESTs 2.06 302962 AI693349 Hs. 228981 EST 2.06 332446 AA112799 Hs. 238756 ESTs; Weakly similar to unknown [H.sapie 2.06 334972 CH22_FGENES.468_2 2.05 330196 CH.05_p2 gi|6165140 2.05 304754 AA579795 EST singleton (not in UniGene) with exon 2.05 309726 AW248521 Hs. 195188 glyceraldehyde-3-phosphate dehydrogenase 2.05 333939 CH22_FGENES.301_5 2.05 304836 AA587008 EST singleton (not in UniGene) with exon 2.05 302087 AA324163 EST cluster (not in UniGene) with exon h 2.05 308424 AI650714 EST singleton (not in UniGene) with exon 2.05 304347 AA176914 EST singleton (not in UniGene) with exon 2.05 333141 CH22_FGENES.85._1 2.05 310573 AW292180 Hs. 156142 ESTs 2.05 337565 CH22_C65E1.GENSCAN.1-11 2.05 304295 AA084082 EST singleton (not in UniGene) with exon 2.05 326624 CH.20_hs gi|5867553 2.05 326443 CH.19_hs gi|5867385 2.04 339012 CH22_DA59H18.GENSCAN.19-2 2.04 337384 CH22_FGENES.745-1 2.04 332326 T79623 Hs. 111787 ESTs 2.04 303706 AW501525 EST cluster (not in UniGene) with exon h 2.04 336046 CH22_FGENES.679_8 2.04 301770 R05887 EST cluster (not in UniGene) with exon h 2.04 326726 CH.20_hs gi|5867597 2.04 330485 M11186 Hs. 113216 oxytocin; prepro-(neurophysin I) 2.04 332956 CH22_FGENES.48_13 2.04 300021 M97935 AFFX control: STAT1 2.04 306872 AI086920 EST singleton (not in UniGene) with exon 2.03 302744 L03151 EST cluster (not in UniGene) with exon h 2.03 338507 CH22_EM: AC005500.GENSCAN.390-11 2.03 334020 CH22_FGENES.317_1 2.03 333870 CH22_FGENES.291_3 2.03 330552 U40223 Hs. 248157 pyrimidinergic receptor P2Y; G-protein c 2.03 335486 CH22_FGENES.570_18 2.03 339374 CH22_BA232E17.GENSCAN.2-5 2.03 328384 CH.07_hs gi|5868392 2.03 334690 CH22_FGENES.420_3 2.03 310318 AI733942 Hs. 145338 ESTs 2.03 325893 CH.16_hs gi|5867088 2.03 331373 AA435513 Hs. 178170 ESTs; Weakly similar to DUAL SPECIFICITY 2.03 329784 CH.14_p2 gi|5912597 2.03 335087 CH22_FGENES.488_11 2.03 310582 AI336563 Hs. 254585 ESTs 2.03 332611 R06751 Hs. 1600 chaperonin containing TCP1; subunit 5 (e 2.03 339258 CH22_BA354I12.GENSCAN.8-3 2.03 336851 CH22_FGENES.274-1 2.03 305596 AA780664 Hs. 8734 ESTs; Moderately similar to !!!! ALU CLA 2.03 330364 CH.X_p2 gi|3126882 2.03 302940 AL137619 EST cluster (not in UniGene) with exon h 2.03 317349 AA923657 Hs. 126359 ESTs; Weakly similar to !!!! ALU SUBFAMI 2.03 309869 AW300314 EST singleton (not in UniGene) with exon 2.03 333422 CH22_FGENES.147_2 2.03 325233 CH.10_hs gi|6381943 2.03 330586 U77968 Hs. 79564 neuronal PAS domain protein 1 2.03 336725 CH22_FGENES.88-1 2.02 334157 CH22_FGENES.340_7 2.02 303357 AW006352 Hs. 159643 ESTs; Weakly similar to MLD [H. sapiens] 2.02 328533 CH.07_hs gi|5868482 2.02 309210 AI962817 EST singleton (not in UniGene) with exon 2.02 327412 CH.02_hs gi|5867750 2.02 333172 CH22_FGENES.94_7 2.02 334869 CH22_FGENES.447_3 2.02 301047 AA971465 Hs. 116136 ESTs 2.02 329394 CH.X_hs gi|6478817 2.02 301736 F12128 EST cluster (not in UniGene) with exon h 2.02 335591 CH22_FGENES.581_30 2.02 338234 CH22_EM: AC005500.GENSCAN.260-7 2.02 334433 CH22_FGENES.385_8 2.02 334904 CH22_FGENES.452_18 2.02 318443 AI939323 Hs. 157714 ESTs; Weakly similar to NEUR ACETYLCHOLI 2.02 300151 AI243445 Hs. 189654 ESTs 2.01 310348 AI478563 Hs. 145519 ESTs 2.01 310898 AI439868 Hs. 165742 ESTs 2.01 332860 CH22_FGENES.27_3 2.01 301699 AI879117 EST cluster (not in UniGene) with exon h 2.01 332554 W96450 Hs. 23111 phenylalanine-tRNA synthetase-like 2.01 327994 CH.06_hs gi|5868218 2.01 315613 AW137420 Hs. 192311 ESTs 2.01 335356 CH22_FGENES.541_3 2.01 334028 CH22_FGENES.318_7 2.01 335277 CH22_FGENES.523_3 2.01 308657 AI749855 Hs. 236497 EST; Weakly similar to GLANDULAR KALLIKR 2.01 305913 AA876109 EST singleton (not in UniGene) with exon 2.01 323681 AW247730 Hs. 102548 glucocorticoid receptor DNA binding fact 2.01 333533 CH22_FGENES.175_20 2.01 328753 CH.07_hs gi|5868298 2.01 302397 L01694 Hs. 211523 guanine nucleotide binding protein (G pr 2.01 304643 AA526588 EST singleton (not in UniGene) with exon 2.01 333065 CH22_FGENES.75_8 2.01 316192 AA904441 Hs. 221286 ESTs 2 302533 L36149 Hs. 248116 chemokine (C motif) XC receptor 1 2 312988 AA813689 Hs. 123436 ESTs 2 333612 CH22_FGENES.217_7 2 333615 CH22_FGENES.217_10 2 316085 AI027959 Hs. 132300 ESTs 2 337936 CH22_EM: AC005500.GENSCAN.85-7 2 330972 H18467 Hs. 118983 ESTs; Weakly similar to diaphanous 1 [H. 2

[0346] TABLE 20 B survivor vs Mets - Up in Mets Pkey Ex Accn UniG_ID Complete Title Ratio BS/Met 316625 AA780307 Hs. 122156 ESTs 0.28 316076 AW297895 Hs. 116424 ESTs 0.3 315943 AA699756 Hs. 117335 ESTs 0.38 317198 AI810384 Hs. 128025 ESTs 0.38 320082 AA487678 Hs. 189738 ESTs 0.39 313510 AI147291 Hs. 154006 ESTs 0.39 323683 AI380045 Hs. 225033 ESTs 0.39 318558 AW402677 Hs. 90372 ESTs 0.4 310264 AI915771 Hs. 148867 ESTs 0.4 314945 AW276866 Hs. 192715 ESTs 0.41 313403 W86995 Hs. 113157 ESTs 0.42 321505 H73183 Hs. 129885 ESTs 0.43 312171 AW444619 Hs. 138211 ESTs 0.43 324585 AI823969 Hs. 132678 ESTs 0.44 316695 AA809844 EST cluster 0.44 (not in UniGene) 319818 AA825819 Hs. 136952 ESTs 0.44 337522 CH22_(—) 0.45 FGENES.819-1 324714 AA574312 Hs. 245737 ESTs 0.45 315060 AA551104 Hs. 189048 ESTs 0.46 300548 AI026836 Hs. 114689 ESTs 0.47 304483 AA431441 EST singleton 0.47 (not in UniGene) with exon 313096 AI422367 Hs. 163533 ESTs 0.47 306501 AA987294 EST singleton 0.47 (not in UniGene) with exon 329086 CH.X_hs 0.47 gi|5868604 320176 AA167566 Hs. 133325 ESTs 0.47 320418 AI674461 Hs. 199638 ESTs 0.47 302982 W92391 Hs. 198222 ESTs; 0.48 Weakly similar to C2H2-type zinc f 315609 AW207535 Hs. 224012 ESTs 0.48 317056 AA904908 Hs. 250643 ESTs 0.48 314361 AL038765 Hs. 161304 ESTs 0.49 315169 AI371390 Hs. 158667 ESTs 0.49 323743 AA324992 Hs. 257168 ESTs 0.49 313903 AW167439 Hs. 190651 ESTs 0.49 315061 AA551196 Hs. 188952 ESTs 0.49 300969 AI140799 Hs. 76230 ribosomal 0.5 protein S10 331950 AA454595 Hs. 99369 ESTs 0.5 315076 AI623817 Hs. 168457 ESTs 0.5 300975 AI283548 Hs. 149668 ESTs 0.5

[0347] TABLE 1-20A Pkey CAT Number Accesssion 108446 112224_1 AA085383 AA126091 AA074174 AA075373 AA079120 AA070831 AA075978 AA075372 AA128503 108474 116896_1 AA115179 AA079667 AA115897 AA079771 100635 10605_34 BE259039 W29128 AW410299 X72990 BE246492 NM_005243 X66899 AI909006 AW248151 AL031186 AA012966 BE273549 BE311429 BE253102 Y07848 BE538102 BE256863 BE261240 BE312156 BE618412 BE257322 BE620446 AW806629 AA376777 AA325384 BE256808 BE251039 BE257878 BE275352 AA357169 AW403562 AA204995 AA093259 W95953 BE256279 BE336683 BE252465 BE251266 AA380754 BE294942 AA380941 AA380999 BE297164 BE249995 BE294719 BE295372 AI270673 BE305132 BE563752 BE295357 AI525421 BE263980 AA057505 AA020915 BE266318 BE206948 AI474020 BE296420 BE297374 BE408545 BE019366 BE407372 BE266180 BE279437 R58233 T19567 BE300738 AW381179 AA357571 AW361285 AA436908 AA301019 AA301022 N20202 BE408777 BE548638 BE167415 AA071260 BE088429 BE280092 W23117 T19568 R51681 AW402216 W22784 BE185607 AI457224 BE544120 AL134874 S72620 AA375079 D51319 AW818280 BE514686 AW853024 BE563744 AA300469 T07592 BE622190 BE272834 W21781 BE315450 BE542367 BE393120 AA988441 H55137 BE562296 BE622502 BE395960 AA329733 AA332348 AI768317 AA456866 AI497832 AW878437 AA857042 U18018 BE621418 AI818790 AI949507 BE397693 AI885545 AI858854 AI355147 BE169028 S62138 AW732191 AA856891 BE266060 X71427 BE268557 AF095890 AW001288 AI799634 AI623498 AA071346 BE547662 BE261446 AI564543 BE559759 U35622 BE314249 BE264915 AI638591 AI538385 AW090025 BE384754 AI888689 AW778800 AI925273 AA075797 AW949130 AV660275 AW438697 AI587137 AI524121 AA806249 AW628247 AA808241 AI244388 AI761125 AW117672 AA911782 AI129250 AA654447 H55291 BE258050 BE206162 W95867 AA857187 AI871378 AI660103 AW103827 AI220929 AW149949 BE465561 AI302857 AW168841 D82190 AW249814 AI623432 AI687358 AW951077 R51592 W60458 AI092863 AW474693 D12765 AI911646 D82208 D82187 AW074031 AI358527 AW338497 AA970893 AW072573 AA205364 AI858886 AA012830 AW148763 AI863056 AA548656 BE250325 AI016994 AI864005 BE046122 AI497746 C75340 R58896 D82141 AW168240 C19048 AI741090 D29465 AI222365 AA948288 AI583522 AW572212 AI091290 AA582727 AA579897 AA570629 W60883 AW516989 AL038160 AA577334 AI865872 AA994043 AA922583 AA464778 AA209178 AI829479 AI370235 BE246529 AA384177 AA456255 AI699730 W60654 AL035744 AA862042 R32756 AI886886 AA993087 AI289479 AA627840 AA464184 AI619503 R32755 AW075358 AI432315 AA457024 AA020865 R92132 AA454629 AA746059 AA454643 AA456240 AA826984 BE163738 AI806470 AI991074 AI802560 AA587095 AA558714 AA968521 N87780 AI538246 N71794 AV661738 AI368903 AA362570 AI989445 AI674962 S75762 BE245204 AA975296 D20123 AW005704 AA693328 AA582270 AI918474 AW205707 AI696299 AA220990 AA101538 T29030 H27201 AW262526 AI610530 AA126840 AA126790 X92120 AW367868 BE299644 BE299451 AA476561 BE300044 AA134363 BE295222 AA307504 N42337 AA319098 N39502 AW964461 N57241 BE299049 N86332 R51156 AA085859 T75212 AA133939 AA147129 AA156161 BE543953 BE538848 AA133676 BE299745 AA135050 AA218535 AW406401 AW411287 BE410528 C01410 NM_004083 BE314959 AA836413 AA085862 AW024370 AA471059 AW467508 AA001025 AI828231 AA633221 T95517 AA147038 AA476447 AW027012 AW078627 BE513200 AI192297 AA886279 AW081806 AA316185 AA010506 AI269929 W93139 AI682935 AA609555 AA378028 AI093877 AA999997 AA730698 AI143923 AW575315 AA890550 AA494353 AW576601 AI796336 AA826130 AA609207 AI539618 AI088539 AI089090 AA825505 AA632978 AA015892 AW204713 AA156495 AA824613 AA133630 N29826 AA527476 AI633352 T27908 AA134364 AA133940 AW043601 H37775 AA772375 AA057871 AA047888 AA054225 H86568 AA001511 H25718 AW189507 AA165589 AA054433 H85549 AA165486 AA058972 AA454911 AA464064 AA493802 AA428253 R85508 AW302469 AI611812 BE162582 F11073 T95518 N26811 AI783929 H40669 AW611745 AI658803 R51042 R45276 AA528386 AA782875 AW880218 AL138391 AA314536 AW949338 AA149466 AA149552 AI346513 AA216776 BE349131 AW007654 AI141803 AA622688 AI185131 AW057635 AA101539 AA627986 H27202 AI536847 W93084 AI973148 AI246788 AW572108 AI469414 AA454835 AA612707 AA430746 AI084991 AA010400 AA856636 AA463928 AI248310 R07170 AA834033 D12244 AI655670 AA054350 AA639480 AI702067 AI475389 100643 3931_1 NM_005032 M34427 AA332167 AW409711 AL119718 BE297581 BE299855 AA082284 AA226855 AA149568 AW391953 M22299 BE163594 AW847881 AW366993 BE142871 AW847885 AW604137 AW847753 AW847886 AW376442 U48350 AW607478 AA373011 AA334080 BE294177 AL121355 AA302236 BE540666 BE170588 AA346884 BE541512 AA226818 AA082001 AA366490 AW604122 AA205784 AW607791 BE168496 AA058497 T64373 BE165633 AW802804 AW847878 AA187408 AA088397 AI751745 AA344103 AA034463 AI906008 AA363580 AA379193 AI332642 AI143569 W52748 W52754 AA385532 AA085967 F05943 AA363422 AA133444 AA133477 AA029541 N48387 N83348 AA376066 AA147671 W70187 AA316255 BE174987 AA452776 AA089605 AL047776 BE162673 H39532 BE168406 AA357654 AA328728 AW813442 D57844 AW839748 AW839663 D57357 AA334536 AW268674 AW950788 AW409888 AI160544 D57821 AW664382 D25884 AI755101 AW130365 AI609094 AI984064 AI806523 AA492516 AI755258 BE157210 AA374884 AI983923 AI831088 AA706501 AI754957 AI688651 AI088623 AI336114 N38752 T56004 AA845200 AA858377 BE157397 AW069347 AA045366 AW316918 AW130372 AI355398 BE157396 AI751746 AI375820 AA129935 W60002 N24781 AI805924 W60009 AA044283 AA121161 AI539277 AA301885 AW019944 AA133445 AA101108 AA033559 W70060 AA617751 AI986261 AI023234 D82235 AA085846 AW754181 D82093 D82100 AA147653 AA600256 D57884 AI753982 AI568050 AI146490 AW302280 AI433051 AA329188 AW572150 AW166345 AI337981 AA778973 N67577 AA227207 AA838281 C06190 AL046997 AI217662 AI752979 AW627538 AI127171 AI440461 T64184 AA845190 AA227111 AA877394 R60962 AA505646 AA770545 AI696264 AA953747 AA904094 AA058318 D57026 T17158 AA578545 AW085082 BE148939 AW815069 BE152843 BE149068 BE149036 AW815073 AW753691 BE149040 AW815065 BE152842 BE149072 AW753692 AW815055 BE152837 BE152849 BE152840 AW815070 BE152829 BE152846 BE148972 BE149042 BE149074 AW753668 BE152832 BE152841 BE149082 BE149050 AA347261 BE152852 BE152847 R65797 F02189 AA483448 AI954410 AA865375 BE152836 BE152838 BE152839 T17300 BE152844 BE152833 BE152834 AA029542 AI567601 AI362353 BE162140 AI381384 BE152851 D57038 D57043 AI418363 AA133478 BE149051 BE149083 BE152850 BE149052 BE149084 AA886686 BE149064 BE149032 AA044093 AA129934 AA303976 BE157211 AA187291 BE152830 AA046552 BE149047 BE149079 BE149033 BE149065 BE149044 BE149076 BE149053 BE149085 BE149034 BE149066 BE149048 BE149080 BE149038 BE149070 BE149045 BE149077 100670 22023_1 AA332178 BE259177 BE545625 T09105 S62076 M16424 NM_000520 BE244309 F13516 BE251567 BE514981 AL119537 AA336739 BE261801 AA278642 N32708 T77034 W24621 W42478 AW630382 AW856214 AA134234 M13520 BE379212 AA287459 BE019379 BE297192 BE162970 AW405668 AW403322 BE272280 BE208703 BE304428 BE162807 BE162828 BE162887 BE078944 BE163025 BE162878 BE162909 BE162898 BE162791 BE162880 BE073563 BE163086 BE162896 BE162770 BE073565 BE162906 BE162913 BE162947 BE162803 BE262199 BE162811 BE080697 BE315095 AW206024 AI291054 BE087364 AL046839 AA304422 AA847660 AA669876 BE392765 AI567798 AW026644 AW151258 AA996314 AI828660 AI571158 T61941 AW103503 AW172698 AI923115 AI823709 T62167 AW771381 AW151782 AI799284 AW242271 AA128031 BE261306 BE312241 AI674880 BE261057 AA630684 AA831305 AI139546 AW082447 AA916854 AA916855 T05970 AA599395 AA921680 AI244674 AI041920 AA424998 AI362999 W42543 T51260 AI362486 AI699366 AI827925 AI027381 AI027370 AI209049 AA782220 AI334014 AI279051 AI217711 AI674210 AI193370 AI701683 T23782 AI927545 AI784291 AA128007 AI370630 AI972736 AA853763 N92379 AI916746 AA639633 AA907603 AI479452 AW950971 T28985 AI685825 AA563654 AA745291 AW089417 F10858 AI354227 R38108 AI668647 AA994088 AI740910 AW880973 AI739410 AI480346 N78987 AI473892 BE162903 BE254430 BE260426 AA650012 AW006426 100673 21517_2 AW403342 AW248986 BE561709 AA357312 BE311834 BE389496 BE294887 AW732696 BE047868 AI702383 BE019155 AI702367 BE408966 BE280458 BE313759 BE513492 BE535404 BE280258 AC005263 NM_007165 L21990 AW732711 AI564920 AW249094 BE265365 AW607186 AW607346 BE005217 H27211 U46230 BE260066 BE207043 BE546782 AW248659 108559 41469_9 AA085228 AA085161 108569 118606_1 AA082885 AA114265 AA085398 AA113184 100700 17137_1 AA932794 BE540417 AW409802 AW410765 BE296651 BE294197 BE164813 AW381886 AW381806 AL048654 AW403058 BE207228 AA464654 AW966967 AA326831 BE407277 BE408669 AA476527 AA115576 AA359697 AA476357 AA449939 BE263719 AL045304 W21442 R28919 BE395990 AA252273 AI346812 BE538487 AA507160 W93950 N42025 AI088439 AL134931 AA031524 AI887287 AW470017 AA476423 AA464553 AW410766 AI569421 AA577476 AI248935 AI912371 AW615674 AA824237 AA807746 AA827377 AA890268 AA476309 AI086424 AW409698 AA031553 AW451901 AI520934 AW050554 R49825 N30302 AA532541 W94004 N93402 AA115549 AA331202 L25665 NM_005275 AA436745 AI122671 R49779 R18508 100734 35197_1 AI807481 AI500404 AI092260 BE348962 AI143675 AA772399 AA772398 AI368565 AI379172 AI083781 AI871363 AA843793 NM_000141 M87770 X52832 M55614 Z71929 W05259 AA548551 AI498743 BE081295 BE162251 F05643 AI127918 H83199 W07463 BE551725 R28404 AW206461 AW590506 AI885536 N69800 R93496 R25381 AA443093 AI143063 AI284647 AI703144 AA309032 AA309031 AW949426 AW949428 AI638387 AI638356 R77173 R38513 T89263 F01900 H87979 R70205 AA664355 AA235910 AA033657 AI436212 N50463 AI433805 AI081876 AI421090 AW020818 AI559529 AI887420 BE154202 AA889062 AA723410 BE537575 AA236812 AI218552 AI264866 AI290617 AA424365 AA424505 AW073347 AA032183 AI142488 N55322 AI884363 AI336070 N67307 AA608928 T94993 AW514184 AA724695 N66630 AI379638 AI274671 AW628470 AA235346 AA687581 AI073906 AI263602 AI869111 AI805693 AI423808 AI076491 AI374640 H82967 AA776567 AA256191 T29856 AA953586 AI140801 AI805484 AA984329 R93497 AI017114 AI263355 N81103 AW418776 D57474 AI918460 AA256152 AI683268 AI042628 AW196650 C00195 AI918567 T28903 N95383 R13671 T94939 AI275235 AA235751 T84335 100739 2738_3 M59287 L29222 AI251890 BE244986 AI708332 117040 46956_1 AW970600 AA503323 H89218 AF086031 H89112 100748 41861_1 X06096 X05826 100760 1334_7 AW794626 M27126 M27014 100779 458_127 BE561958 BE561728 BE397612 BE514391 BE269037 BE514207 BE562381 BE514256 BE514403 BE514250 BE397832 BE269598 BE559865 BE396881 BE560031 BE514199 BE560037 BE560454 100787 458_127 BE561958 BE561728 BE397612 BE514391 BE269037 BE514207 BE562381 BE514256 BE514403 BE514250 BE397832 BE269598 BE559865 BE396881 BE560031 BE514199 BE560037 BE560454 130872 21268_1 U61084 NM_904900 U61083 AI761325 AI826909 H79385 T81886 AI222763 N68038 AI281048 H79274 AA603662 AA721720 T71211 C00488 AA994672 AW136970 AW368715 AA380767 AL022318 108641 853_−13 AA112059 100818 19604_3 U79251 AA843851 R38201 R66461 R44908 AA683289 H17477 R37364 R52832 AW298336 AA351391 NM_002545 L34774 AA296886 AW967001 T28889 R13451 T77331 AL119196 AL118830 H08459 AW892812 AW905838 H17585 R52878 130930 2773_1 NK_005658 U19261 BE622108 AA313592 AW950162 H25107 R71725 R50630 AI524201 AI476301 AW014547 AW195770 AI378122 AI554908 AI927196 AI913959 AW044513 R50534 AI379950 AI311593 BE043305 R82981 AA769375 R77429 AW196220 AI269033 AA883433 R71691 F11489 AW771234 AA402642 AA399408 AW771244 AI400707 R55446 124394 5590_5 AI950447 AW027427 AI640151 AI139433 AI400708 AW779975 AI739122 AI384000 AW079410 AI473425 AA150109 AI766579 AI351784 AI209046 AI474732 N29724 AI382653 100882 458_127 BE561958 BE561728 BE397612 BE514391 BE269037 BE514207 BE562381 BE514256 BE514403 BE514250 BE397832 BE269598 BE559865 BE396881 BE560031 BE514199 BE560037 BE560454 100885 12707_3 X07881 NM_006249 X07637 AA376715 AA376677 X07715 X07704 S80916 100896 205_6 M91803 X65362 100898 8542_1 BE387614 R51501 AA199714 AW674779 F08178 BE269071 AA376313 H08264 AA380420 H18785 AL042151 BE277758 BE267438 NM_005850 L35013 BE540833 BE390902 BE391494 BE277459 BE385592 BE390612 BE384263 BE387779 BE388647 BE537373 BE547158 AW409585 AW374033 AW602185 AA355725 AW577548 AW935015 AW935160 W40232 AW938647 AW374332 AA434040 BE293488 AL138361 BE560260 AI745075 AA317980 AW949382 AI834311 AI653582 AI831042 AI361878 AA618606 AA729052 AI424969 AA199715 AW769374 AI828422 AW044307 AI862816 AI203583 AW084461 AW514655 AA831883 AA290672 AA831286 AA578510 AW089965 AW150746 AA292743 H22232 AI469275 AW439312 AA292744 AW471443 AI473989 AA593336 AA464070 AI678937 AW069451 AA970763 AA610480 AA593328 AA464009 AA768985 AI298928 AA436600 AA464718 AA699361 D61482 D55935 AI369591 AA470695 AI809135 AA640627 AI568446 R51502 W45467 AI655316 AA463934 AW168609 AW518663 BE045525 Z41251 AI868091 AA908160 AI026697 AI886259 AI612932 AA215437 AI956014 BE541087 BE255652 BE265878 BE394102 W27502 108706 13255_−3 AA121820 108710 133560_1 AA121959 AA121960 108712 14671_1 AA335738 AI817426 AA099503 AA643106 AA650582 AW188499 AA155785 AW024305 AA992590 AW793619 AA121250 H93101 AA994582 AW007456 AW799974 AA535738 AI460362 AI571942 AW517220 BE044613 AI830018 H50382 AW391334 AA741035 AI697291 W37616 AA866185 AW264926 H52854 AW796893 AI660673 AA464961 AI808376 H13850 H81969 W92615 H41636 H73900 H66731 AA281556 AA026801 AA479538 AA588901 AA446262 R86974 H84761 R62958 H70493 AI991716 AI833075 AW800109 R54692 W94542 R78651 AI694890 AW845181 W31325 AA224371 AA359813 AW178868 H53738 F22305 AI874075 AI567440 AA853303 H25886 AA550734 AI874064 AW148463 AI586928 T28979 AW950966 AI828723 AI918890 F16942 AA223763 AA622370 AA630985 AA402644 N70971 AI147210 AW410026 AA485517 AI129376 AW337522 AW136362 AI123362 AI281243 AW339600 AI478990 AI339256 AW768289 AI660065 AI309560 AI141111 AI280844 AI338227 AI310719 AA733112 AA903203 AI073351 AI348225 AA974151 AI141386 AI311925 AI042124 AI193176 AI186999 AI735528 AI335702 BE550806 W47157 W70086 W44788 AI218741 AI074049 AI168088 AW050904 AI083978 AI131084 AW328532 AI969255 AA069140 AA328735 F20431 AI625929 AA621514 AA384576 H98823 AI371848 AI360520 AW079514 AW845177 AA948626 N52236 AA464158 H43126 AA465035 AA464221 AA365164 AI539264 AW250430 N27769 AA157036 AI124029 AI635488 AA374090 AA515126 AA614763 AI872210 AI160916 AI002016 AA813669 AA190550 AI262671 AI460058 AI690719 AA805473 AA523207 AA477649 H13898 AI056086 H42356 R32267 R99431 AA481898 AI130779 AA769777 AA910293 AI284079 AA936692 AA903953 AA947753 AI568924 AA902966 AA807082 AA489337 N58247 AA872223 AA485362 AA024906 AI092224 AA443621 AA603059 N58248 AA927262 AA329524 AA026369 N73450 AI244031 AI192676 N25190 W32248 W32324 AI284307 AA074470 N33116 AA947399 H52855 T52343 AA643260 AA573752 AI031889 AA877690 AA531409 X13710 AI500538 R32315 BE168562 AA401993 AA883251 W37615 AA305694 W78964 AA024905 H53678 W47278 AA224423 AA371881 AA335679 AA336008 T52416 H69646 AA300266 AA325728 N73204 N77626 R54691 W24032 AA868340 BE407766 H81968 W46665 AA883934 AA187290 AW571425 AI280505 AI079662 AI470373 AA991617 AA173165 AI244032 AA922440 AA856918 W80458 AA121251 AI160062 H50349 T67744 W46574 AA969287 W01485 BE615302 BE388184 AA314246 H85693 W31948 AV650437 AW160467 W44891 AA723773 AW328531 AA313224 AA299527 R86894 AA312505 H21582 AA157493 H78480 N36060 N77627 BE218674 W02853 AW954844 AA429974 BE382847 AI541225 H93229 BE281553 AA147790 AA327374 AW839840 AA969229 R99337 BE278812 AI190450 AA479549 AA156012 R78705 AA224081 N44944 D56066 AA969012 AW178878 AW105500 N52391 AA622301 AA858204 AI290372 AI205676 H51289 AA548013 BE544240 AA280160 BE170901 AI192429 R77056 AA310925 AI219128 AA121993 AA070432 R63012 108785 4962_−6 AA128946 102156 33676_1 H08948 AA353935 R14985 U17977 H15387 F05567 R88476 AW968314 R89646 R87941 AA258917 AW895155 AW947450 AA223175 AA223559 W92508 W02327 AA322882 AW960879 H39040 H39039 R90891 AA580343 BE155037 BE154984 N40110 AL137683 BE265131 R17329 AL096733 M79202 AA625234 AA427472 AW361296 AA658045 AA322177 R54596 AA171880 AL042331 U18920 AA298036 AW051888 AI378803 AW601640 AI885103 AA297019 AI192706 AW055183 BE312004 H42382 AA534726 AA205943 AA204817 AA298966 AW015511 AA223176 H08864 AW028026 R45676 AI023345 AW263046 AI161297 AI168747 AW024885 AI832106 R88436 R86849 W92509 AA857908 N26989 AI589169 AI570370 AA223525 AA171552 AA405862 AW001095 AI864651 H39060 AA776342 AI682761 AA768233 R86855 AI367878 R42675 AA832040 R89042 AI984848 AI524629 AI289021 AW014020 AI241757 AI421241 AA430654 AI360728 AW299692 AA258155 AA782959 AI684411 AA531501 H41286 AI125231 H15388 M62002 R88819 AI203108 Z38537 AI432593 AA887767 AW023638 H39016 AI424700 102186 33745_1 U20285 AW674959 W69617 NM_004127 AU076538 BE245805 AW250694 AW248164 BE294678 AA298083 BE266030 BE262348 AL038115 BE253256 AA330082 AW401492 BE070159 BE619216 AW379955 AW379968 BE266381 AL046753 AW379969 Z45804 H12155 BE543514 Z44978 AA026010 AA776140 AA337940 AA315980 AA308668 BE156554 R33383 BE271569 BE378456 AA972517 AW748739 R73336 AA302223 AA279618 BE561802 AI693878 BE560858 BE513865 BE267975 R36064 AI056387 AI961737 AW167515 AA280965 AI479985 AI859762 AA309009 AA573934 AI669053 BE046497 H14545 BE222639 AI910094 AA484398 AA521025 AA807224 AW247126 AW732050 AA377850 AW951499 R73316 AI458542 AI564292 AA974663 AI951858 AA595162 AI685726 AA604679 AI813703 AI091930 AI567797 AI521316 AI377236 AA583446 W79901 AI743281 AA913078 AI139695 AA994505 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CH22_2994FG_584_14_LINK_E 328420 c_7_hs 328428 c_7_hs 335651 CH22_3011FG_590_2_LINK_EM 335652 CH22_3012FG_590_3_LINK_EM 328436 c_7_hs 328444 c_7_hs 335667 CH22_3027FG_590_18_LINK_E 328462 c_7_hs 328467 c_7_hs 335687 CH22_3048FG_596_2_LINK_EM 335690 CH22_3051FG_596_5_LINK_EM 328474 c_7_hs 335692 CH22_3053FG_596_7_LINK_EM 335693 CH22_3054FG_596_8_LINK_EM 328484 c_7_hs 335700 CH22_3061FG_598_1_LINK_EM 305621 AA789095 305632 AA805276 335720 CH22_3081FG_599_23_LINK_E 335721 CH22_3082FG_599_24_LINK_E 328504 c_7_hs 328506 c_7_hs 328507 c_7_hs 335733 CH22_3095FG_601_3_LINK_EM 335739 CH22_3102FG_601_10_LINK_E 335745 CH22_3108FG_601_16_LINK_E 335747 CH22_3111FG_601_20_LINK_E 335750 CH22_3115FG_602_4_LINK_EM 335755 CH22_3122FG_604_4_LINK_EM 328544 c_7_hs 335768 CH22_3137FG_607_2_LINK_EM 305686 AA812726 328552 c_7_hs 335774 CH22_3143FG_607_10_LINK_E 328557 c_7_hs 328558 c_7_hs 335777 CH22_3146FG_607_13_LINK_E 305697 AA814956 335782 CH22_3151FG_609_4_LINK_EM 335783 CH22_3152FG_610_3_LINK_EM 328589 c_7_hs 335787 CH22_3156FG_611_3_LINK_EM 328570 c_7_hs 328581 c_7_hs 328582 c_7_hs 328592 c_7_hs 337011 CH22_4876FG_427_6_(—) 337023 CH22_4894FG_433_12_(—) 337032 CH22_4910FG_438_3_(—) 337069 CH22_4967FG_448_2_(—) 337092 CH22_5016FG_465_12_(—) 337093 CH22_5017FG_465_18_(—) 337094 CH22_5018FG_465_19_(—) 337097 CH22_5028FG_471_1_(—) 305700 AA815428 335806 CH22_3178FG_616_8_LINK_EM 335817 CH22_3189FG_618_5_LINK_EM 328607 c_7_hs 335827 CH22_3200FG_620_1_LINK_EM 335831 CH22_3204FG_620_5_LINK_EM 335832 CH22_3205FG_620_6_LINK_EM 328620 c_7_hs 328624 c_7_hs 328636 c_7_hs 335863 CH22_3238FG_629_8_LINK_EM 305782 AA844730 305787 AA845035 328662 c_7_hs 335895 CH22_3272FG_635_3_LINK_EM 337100 CH22_5031FG_472_3_(—) 337114 CH22_5060FG_494_17_(—) 337121 CH22_5096FG_519_1_(—) 337132 CH22_5112FG_526_3_(—) 337168 CH22_5188FG_562_28_(—) 307085 AI160868 337170 CH22_5190FG_564_1_(—) 337172 CH22_5192FG_565_2_(—) 307090 AI161024 305803 AA846052 305808 AA853958 305816 AA854776 335902 CH22_3279FG_635_10_LINK_E 335920 CH22_3297FG_636_16_LINK_E 305841 AA860348 305867 AA864572 335956 CH22_3334FG_647_3_LINK_DJ 305877 AA865649 335968 CH22_3347FG_652_1_LINK_DJ 335971 CH22_3350FG_652_4_LINK_DJ 335975 CH22_3354FG_652_9_LINK_DJ 335980 CH22_3360FG_653_2_LINK_DJ 328768 c_7_hs 328770 c_7_hs 335993 CH22_3373FG_656_6_LINK_DJ 335998 CH22_3379FG_656_16_LINK_D 335999 CH22_3380FG_657_1_LINK_DJ 328791 c_7_hs 337203 CH22_5256FG_591_3_(—) 337204 CH22_5261FG_595_1_(—) 307120 AI184343 307140 AI185762 307177 AI188864 305903 AA873085 305925 AA877883 328803 c_7_hs 330002 c16_p2 328810 c_7_hs 328820 c_7_hs 330021 c16_p2 305967 AA886428 328835 c_7_hs 305971 AA886874 328841 c_7_hs 305984 AA887654 328851 c_7_hs 328859 c_7_hs 330057 c17_p2 330058 c17_p2 305999 AA889603 307215 AI193189 307262 AI202100 307318 AI208577 307380 AI222985 307433 AI244895 307437 AI245683 307556 AI281651 307558 AI281998 337645 CH22_5960FG_LINK_EM: AC00 337657 CH22_5976FG_LINK_EM: AC00 307574 AI283549 307588 AI285535 307592 AI285739 337685 CH22_6020FG_LINK_EM: AC00 337695 CH22_6033FG_LINK_EM: AC00 337697 CH22_6037FG_LINK_EM: AC00 307606 AI290006 307629 AI300246 307642 AI302103 307643 AI302124 307646 AI302236 307703 AI318588 307728 AI335557 307752 AI339447 307799 AI351112 309005 AI884454 307864 AI367417 307877 AI368880 307899 AI380270 309108 AI925949 309169 AI949216 309181 AI951727 307904 AI381019 307912 AI382224 307918 AI383496 307954 AI419692 307961 AI421059 307992 AI434166 309206 AI961962 309233 AI971416 309245 AI972447 309247 AI972768 309275 AI989570 309324 AW015373 309333 AW025709 309343 AW028652 309351 AW057547 309403 AW082954 309533 AW151131 309592 AW172384 325271 c11_hs 325285 c11_hs 325289 c11_hs 309600 AW182066 309605 AW182800 309759 AW268822 309767 AW271805 309815 AW292760 309859 AW298760 302681 31257_1 X97550 X97552 302683 31326_1 X85153 T63701 309958 AW444488 309977 AW451663 309985 AW452919 302727 32493_1 L10141 L10151 L10148 L09095 302747 32813_1 AF062275 L03830 304022 T02990 304055 R07994 304056 R08577 304060 T61464 304125 H40976 304127 H42981 304134 H54627 304195 N35382 302952 39444_1 AF103179 U82961 302996 41196_1 AF054663 AF124197 R70292 304269 AA069029 304324 AA137045 304330 AA157834 304424 AA293494 304465 AA421948 304467 AA424703 304480 AA430373 304485 AA434076 304487 AA434241 304559 AA488050 304575 AA496437 304605 AA513225 304612 AA514207 304623 AA521331 304635 AA523976 304667 AA535602 304674 AA541735 304675 AA541740 304693 AA554263 304696 AA554758 304707 AA564846 304731 AA576085 304734 AA576428 304745 AA577771 304746 AA577793 306009 AA894560 306012 AA896989 306053 AA905312 306081 AA908472 306090 AA908609 304811 AA584361 304813 AA584540 304817 AA584712 304833 AA586504 304841 AA587541 304887 AA599355 306137 AA916176 306180 AA922503 306183 AA922622 306193 AA923457 304918 AA602697 304968 AA614308 306200 AA926816 306220 AA928363 306221 AA928686 306300 AA937573 320789 252516_1 R78712 AA603646 R78713 306351 AA961356 330435 41165_1 U63836 AW842139 X74956 U78550 AW840802 X74954 AW388241 AW842709 AF253321 X74955 X74370 AW363799 BE073386 AI791962 AA587390 AW840865 330436 10605_34 BE259039 W29128 AW410299 X72990 BE246492 NM_005243 X66899 AI909006 AW248151 AL031186 AA012966 BE273549 BE311429 BE253102 Y07848 BE538102 BE256863 BE261240 BE312156 BE618412 BE257322 BE620446 AW806629 AA376777 AA325384 BE256808 BE251039 BE257878 BE275352 AA357169 AW403562 AA204995 AA093259 W95953 BE256279 BE336683 BE252465 BE251266 AA380754 BE294942 AA380941 AA380999 BE297164 BE249995 BE294719 BE295372 AI270673 BE305132 BE563752 BE295357 AI525421 BE263980 AA057505 AA020915 BE266318 BE206948 AI474020 BE296420 BE297374 BE408545 BE019366 BE407372 BE266180 BE279437 R58233 T19567 BE300738 AW381179 AA357571 AW361285 AA436908 AA301019 AA301022 N20202 BE408777 BE548638 BE167415 AA071260 BE088429 BE280092 W23117 T19568 R51681 AW402216 W22784 BE185607 AI457224 BE544120 AL134874 S72620 AA375079 D51319 AW818280 BE514686 AW853024 BE563744 AA300469 T07592 BE622190 BE272834 W21781 BE315450 BE542367 BE393120 AA988441 H55137 BE562296 BE622502 BE395960 AA329733 AA332348 AI768317 AA456866 AI497832 AW878437 AA857042 U18018 BE621418 AI818790 AI949507 BE397693 AI885545 AI858854 AI355147 BE169028 S62138 AW732191 AA856891 BE266060 X71427 BE268557 AF095890 AW001288 AI799634 AI623498 AA071346 BE547662 BE261446 AI564543 BE559759 U35622 BE314249 BE264915 AI638591 AI538385 AW090025 BE384754 AI888689 AW778800 AI925273 AA075797 AW949130 AV660275 AW438697 AI587137 AI524121 AA806249 AW628247 AA808241 AI244388 AI761125 AW117672 AA911782 AI129250 AA654447 H55291 BE258050 BE206162 W95867 AA857187 AI871378 AI660103 AW103827 AI220929 AW149949 BE465561 AI302857 AW168841 D82190 AW249814 AI623432 AI687358 AW951077 R51592 W60458 AI092863 AW474693 D12765 AI911646 D82208 D82187 AW074031 AI358527 AW338497 AA970893 AW072573 AA205364 AI858886 AA012830 AW148763 AI863056 AA548656 BE250325 AI016994 AI864005 BE046122 AI497746 C75340 R58896 D82141 AW168240 C19048 AI741090 D29465 AI222365 AA948288 AI583522 AW572212 AI091290 AA582727 AA579897 AA570629 W60883 AW516989 AL038160 AA577334 AI865872 AA994043 AA922583 AA464778 AA209178 AI829479 AI370235 BE246529 AA384177 AA456255 AI699730 W60654 AL035744 AA862042 R32756 AI886886 AA993087 AI289479 AA627840 AA464184 AI619503 R32755 AW075358 AI432315 AA457024 AA020865 R92132 AA454629 AA746059 AA454643 AA456240 AA826984 BE163738 AI806470 AI991074 AI802560 AA587095 AA558714 AA968521 N87780 AI538246 N71794 AV661738 AI368903 AA362570 AI989445 AI674962 S75762 BE245204 AA975296 D20123 AW005704 AA693328 AA582270 AI918474 AW205707 AI696299 AA220990 AA101538 T29030 H27201 AW262526 AI610530 AA126840 AA126790 X92120 AW367868 BE299644 BE299451 AA476561 BE300044 AA134363 BE295222 AA307504 N42337 AA319098 N39502 AW964461 N57241 BE299049 N86332 R51156 AA085859 T75212 AA133939 AA147129 AA156161 BE543953 BE538848 AA133676 BE299745 AA135050 AA218535 AW406401 AW411287 BE410528 C01410 NM_004083 BE314959 AA836413 AA085862 AW024370 AA471059 AW467508 AA001025 AI828231 AA633221 T95517 AA147038 AA476447 AW027012 AW078627 BE513200 AI192297 AA886279 AW081806 AA316185 AA010506 AI269929 W93139 AI682935 AA609555 AA378028 AI093877 AA999997 AA730698 AI143923 AW575315 AA890550 AA494353 AW576601 AI796336 AA826130 AA609207 AI539618 AI088539 AI089090 AA825505 AA632978 AA015892 AW204713 AA156495 AA824613 AA133630 N29826 AA527476 AI633352 T27908 AA134364 AA133940 AW043601 H37775 AA772375 AA057871 AA047888 AA054225 H86568 AA001511 H25718 AW189507 AA165589 AA054433 H85549 AA165486 AA058972 AA454911 AA464064 AA493802 AA428253 R85508 AW302469 AI611812 BE162582 F11073 T95518 N26811 AI783929 H40669 AW611745 AI658803 R51042 R45276 AA528386 AA782875 AW880218 AL138391 AA314536 AW949338 AA149466 AA149552 AI346513 AA216776 BE349131 AW007654 AI141803 AA622688 AI185131 AW057635 AA101539 AA627986 H27202 AI536847 W93084 AI973148 AI246788 AW572108 AI469414 AA454835 AA612707 AA430746 AI084991 AA010400 AA856636 AA463928 AI248310 R07170 AA834033 D12244 AI655670 AA054350 AA639480 AI702067 AI475389 330527 14558_−15 S77356 330833 103550_1 AA046804 AA046821 330855 111881_1 AA070316 AA079318 332099 genbanK_AA608983 AA608983 332240 genbank_N54803 N54803 # using Clustering and Alignment Tools (DoubleTwist, Oakland California). The Genbank accession numbers for sequences comprising each cluster are listed in the “Accession”column.

[0348] TABLE 1-20B Pkey Ref Strand Nt_position 332792 Dunham, I. et.al. Plus 73381-73768 332843 Dunham, I. et.al. Plus 1142859-1143494 332909 Dunham, I. et.al. Plus 1946582-1946735 332920 Dunham, I. et.al. Plus 2007562-2007785 332947 Dunham, I. et.al. Plus 2431726-2432006 332949 Dunham, I. et.al. Plus 2436245-2436348 332958 Dunham, I. et.al. Plus 2516164-2516310 332992 Dunham, I. et.al. Plus 2699997-2701093 332993 Dunham, I. et.al. Plus 2701550-2701685 333004 Dunham, I. et.al. Plus 2759056-2759165 333006 Dunham, I. et.al. Plus 2762853-2762953 333007 Dunham, I. et.al. Plus 2763569-2763709 333132 Dunham, I. et.al. Plus 3358040-3358153 333133 Dunham, I. et.al. Plus 3360058-3360195 333139 Dunham, I. et.al. Plus 3369495-3369571 333152 Dunham, I. et.al. Plus 3612171-3612354 333205 Dunham, I. et.al. Plus 3942727-3943009 333221 Dunham, I. et.al. Plus 3978070-3978187 333225 Dunham, I. et.al. Plus 3992229-3992386 333245 Dunham, I. et.al. Plus 4157587-4157668 333248 Dunham, I. et.al. Plus 4162041-4162139 333261 Dunham, I. et.al. Plus 4336597-4337752 333272 Dunham, I. et.al. Plus 4381561-4382212 333281 Dunham, I. et.al. Plus 4506230-4506342 333283 Dunham, I. et.al. Plus 4514226-4514360 333288 Dunham, I. et.al. Plus 4516841-4516939 333298 Dunham, I. et.al. Plus 4581537-4581947 333306 Dunham, I. et.al. Plus 5396233-5396310 333382 Dunham, I. et.al. Plus 4905796-4905913 333403 Dunham, I. et.al. Plus 4925140-4925256 333420 Dunham, I. et.al. Plus 4954302-4954465 333428 Dunham, I. et.al. Plus 4973869-4974007 333464 Dunham, I. et.al. Plus 5210762-5211300 333465 Dunham, I. et.al. Plus 5211385-5211858 333488 Dunham, I. et.al. Plus 5396233-5396310 333515 Dunham, I. et.al. Plus 5564299-5564851 333520 Dunham, I. et.al. Plus 5686133-5586296 333566 Dunham, I. et.al. Plus 5954226-5954473 333567 Dunham, I. et.al. Plus 5959139-5959515 333571 Dunham, I. et.al. Plus 6007916-6008058 333572 Dunham, I. et.al. Plus 6026896-6027189 333576 Dunham, I. et.al. Plus 6090345-6090721 333577 Dunham, I. et.al. Plus 6123950-6124281 333580 Dunham, I. et.al. Plus 6142935-6143145 333587 Dunham, I. et.al. Plus 6250599-6250966 333588 Dunham, I. et.al. Plus 6255445-6255779 333591 Dunham, I. et.al. Plus 6285884-6286251 333592 Dunham, I. et.al. Plus 6297731-6297976 333593 Dunham, I. et.al. Plus 6304132-6304428 333594 Dunham, I. et.al. Plus 6308990-6309450 333599 Dunham, I. et.al. Plus 6337885-6338255 333600 Dunham, I. et.al. Plus 6355629-6355925 333601 Dunham, I. et.al. Plus 6360075-6360442 333607 Dunham, I. et.al. Plus 6504431-6504690 333608 Dunham, I. et.al. Plus 6510834-6511130 333619 Dunham, I. et.al. Plus 6562799-6562926 333623 Dunham, I. et.al. Plus 6584559-6584956 333625 Dunham, I. et.al. Plus 6603020-6603310 333626 Dunham, I. et.al. Plus 6614174-6614467 333627 Dunham, I. et.al. Plus 6620584-6620903 333628 Dunham, I. et.al. Plus 6629004-6629233 333629 Dunham, I. et.al. Plus 6636915-6637205 333631 Dunham, I. et.al. Plus 6650904-6651011 333632 Dunham, I. et.al. Plus 6651520-6651658 333635 Dunham, I. et.al. Plus 6663683-6663973 333637 Dunham, I. et.al. Plus 6674968-6675134 333640 Dunham, I. et.al. Plus 6688350-6688624 333642 Dunham, I. et.al. Plus 6708760-6709139 333643 Dunham, I. et.al. Plus 6728053-6728343 333646 Dunham, I. et.al. Plus 6739110-6739379 333647 Dunham, I. et.al. Plus 6772502-6772779 333648 Dunham, I. et.al. Plus 6787465-6787782 333650 Dunham, I. et.al. Plus 6796852-6797128 333652 Dunham, I. et.al. Plus 6809455-6809573 333653 Dunham, I. et.al. Plus 6811130-6811392 333654 Dunham, I. et.al. Plus 6816731-6816993 333656 Dunham, I. et.al. Plus 6822087-6822406 333657 Dunham, I. et.al. Plus 6831369-6831445 333658 Dunham, I. et.al. Plus 6835282-6835474 333668 Dunham, I. et.al. Plus 7011009-7011223 333670 Dunham, I. et.al. Plus 7027945-7028181 333680 Dunham, I. et.al. Plus 7071730-7071794 333682 Dunham, I. et.al. Plus 7076641-7076760 333698 Dunham, I. et.al. Plus 7205279-7205383 333710 Dunham, I. et.al. Plus 7230314-7230476 333717 Dunham, I. et.al. Plus 7308714-7308815 333727 Dunham, I. et.al. Plus 7373219-7373311 333785 Dunham, I. et.al. Plus 7775317-7775415 333791 Dunham, I. et.al. Plus 7795972-7796082 333859 Dunham, I. et.al. Plus 8041203-8041359 333875 Dunham, I. et.al. Plus 8135505-8136179 333879 Dunham, I. et.al. Plus 8146919-8147062 333891 Dunham, I. et.al. Plus 8156437-8156709 333918 Dunham, I. et.al. Plus 8307124-8307215 333929 Dunham, I. et.al. Plus 8479486-8479580 333932 Dunham, I. et.al. Plus 8489124-8489205 333983 Dunham, I. et.al. Plus 8813593-8813668 333987 Dunham, I. et.al. Plus 8824245-8824376 333997 Dunham, I. et.al. Plus 8866668-8867255 334010 Dunham, I. et.al. Plus 8996696-8998236 334015 Dunham, I. et.al. Plus 9055452-9055595 334017 Dunham, I. et.al. Plus 9139516-9139634 334026 Dunham, I. et.al. Plus 9196549-9196681 334030 Dunham, I. et.al. Plus 9288463-9288782 334044 Dunham, I. et.al. Plus 9373898-9374065 334047 Dunham, I. et.al. Plus 9428152-9428211 334055 Dunham, I. et.al. Plus 9662077-9662270 334063 Dunham, I. et.al. Plus 9731991-9732085 334066 Dunham, I. et.al. Plus 9739568-9739680 334068 Dunham, I. et.al. Plus 9746279-9746477 334076 Dunham, I. et.al. Plus 9801613-9801693 334091 Dunham, I. et.al. Plus 9872327-9872527 334106 Dunham, I. et.al. Plus 10261155-10261841 334109 Dunham, I. et.al. Plus 10267679-10267864 334111 Dunham, I. et.al. Plus 10279365-10279531 334115 Dunham, I. et.al. Plus 10316414-10316608 334118 Dunham, I. et.al. Plus 10344273-10344384 334120 Dunham, I. et.al. Plus 10402389-10403196 334135 Dunham, I. et.al. Plus 10457085-10457183 334235 Dunham, I. et.al. Plus 12983601-12983703 334239 Dunham, I. et.al. Plus 13056569-13056693 334244 Dunham, I. et.al. Plus 13159198-13159302 334257 Dunham, I. et.al. Plus 13213243-13213429 334260 Dunham, I. et.al. Plus 13223819-13223968 334298 Dunham, I. et.al. Plus 13424763-13425914 334342 Dunham, I. et.al. Plus 13646844-13646980 334354 Dunham, I. et.al. Plus 13702598-13702747 334430 Dunham, I. et.al. Plus 14269664-14270102 334435 Dunham, I. et.al. Plus 14275597-14275689 334451 Dunham, I. et.al. Plus 14315572-14315741 334504 Dunham, I. et.al. Plus 14510206-14510398 334510 Dunham, I. et.al. Plus 14522303-14522418 334518 Dunham, I. et.al. Plus 14630584-14630669 334525 Dunham, I. et.al. Plus 14781066-14781137 334528 Dunham, I. et.al. Plus 14787558-14787675 334529 Dunham, I. et.al. Plus 14788825-14788971 334565 Dunham, I. et.al. Plus 14989033-14989353 334568 Dunham, I. et.al. Plus 14992698-14993210 334590 Dunham, I. et.al. Plus 15033247-15033753 334612 Dunham, I. et.al. Plus 15170470-15170535 334626 Dunham, I. et.al. Plus 15299954-15300077 334661 Dunham, I. et.al. Plus 15477716-15477786 334664 Dunham, I. et.al. Plus 15501941-15502119 334666 Dunham, I. et.al. Plus 15504203-15504279 334676 Dunham, I. et.al. Plus 15516334-15516412 334677 Dunham, I. et.al. Plus 15517449-15517560 334719 Dunham, I. et.al. Plus 15778859-15779026 334730 Dunham, I. et.al. Plus 15967830-15967934 334797 Dunham, I. et.al. Plus 16383231-16383458 334819 Dunham, I. et.al. Plus 16758514-16758711 334855 Dunham, I. et.al. Plus 18402556-18402735 334900 Dunham, I. et.al. Plus 19315678-19315743 334906 Dunham, I. et.al. Plus 19323493-19323590 334907 Dunham, I. et.al. Plus 19336829-19336938 334914 Dunham, I. et.al. Plus 19495158-19495275 334915 Dunham, I. et.al. Plus 19505267-19506101 334935 Dunham, I. et.al. Plus 20108247-20108373 335019 Dunham, I. et.al. Plus 20689525-20689582 335036 Dunham, I. et.al. Plus 20755250-20756375 335049 Dunham, I. et.al. Plus 20877184-20877309 335081 Dunham, I. et.al. Plus 21113871-21113937 335131 Dunham, I. et.al. Plus 21449834-21450003 335157 Dunham, I. et.al. Plus 21543302-21544341 335163 Dunham, I. et.al. Plus 21583508-21583655 335174 Dunham, I. et.al. Plus 21631301-21631447 335180 Dunham, I. et.al. Plus 21641226-21641603 335188 Dunham, I. et.al. Plus 21669118-21669328 335189 Dunham, I. et.al. Plus 21673403-21673472 335193 Dunham, I. et.al. Plus 21692208-21692362 335200 Dunham, I. et.al. Plus 21743499-21743881 335201 Dunham, I. et.al. Plus 21745249-21745664 335284 Dunham, I. et.al. Plus 22272583-22272712 335311 Dunham, I. et.al. Plus 22501602-22501676 335320 Dunham, I. et.al. Plus 22542132-22542246 335371 Dunham, I. et.al. Plus 22849529-22849808 335377 Dunham, I. et.al. Plus 22869909-22870188 335421 Dunham, I. et.al. Plus 23250433-23250498 335448 Dunham, I. et.al. Plus 23477532-23477831 335451 Dunham, I. et.al. Plus 23480611-23480711 335455 Dunham, I. et.al. Plus 23486127-23486216 335468 Dunham, I. et.al. Plus 23787246-23787367 335470 Dunham, I. et.al. Plus 23812877-23813365 335482 Dunham, I. et.al. Plus 24087956-24088114 335485 Dunham, I. et.al. Plus 24098953-24099123 335517 Dunham, I. et.al. Plus 24226461-24226531 335536 Dunham, I. et.al. Plus 24498783-24499762 335565 Dunham, I. et.al. Plus 24881886-24882470 335585 Dunham, I. et.al. Plus 24988240-24988405 335587 Dunham, I. et.al. Plus 24991457-24991618 335593 Dunham, I. et.al. Plus 25037253-25037370 335634 Dunham, I. et.al. Plus 25163837-25164042 335651 Dunham, I. et.al. Plus 25317560-25317696 335652 Dunham, I. et.al. Plus 25325625-25325883 335667 Dunham, I. et.al. Plus 25345735-25345856 335687 Dunham, I. et.al. Plus 25445952-25446064 335690 Dunham, I. et.al. Plus 25455442-25455625 335692 Dunham, I. et.al. Plus 25468557-25468725 335693 Dunham, I. et.al. Plus 25471363-25471524 335700 Dunham, I. et.al. Plus 25512222-25512890 335720 Dunham, I. et.al. Plus 25596542-25596646 335721 Dunham, I. et.al. Plus 25599118-25599228 335733 Dunham, I. et.al. Plus 25686486-25686626 335739 Dunham, I. et.al. Plus 25698550-25698826 335745 Dunham, I. et.al. Plus 25718164-25718332 335747 Dunham, I. et.al. Plus 25723304-25723494 335783 Dunham, I. et.al. Plus 25941882-25942040 335968 Dunham, I. et.al. Plus 27743843-27744029 335971 Dunham, I. et.al. Plus 27752808-27753017 335975 Dunham, I. et.al. Plus 27801321-27801391 335993 Dunham, I. et.al. Plus 28006396-28006571 335998 Dunham, I. et.al. Plus 28026247-28026356 336011 Dunham, I. et.al. Plus 28570760-28570900 336035 Dunham, I. et.al. Plus 29016748-29017410 336049 Dunham, I. et.al. Plus 29124451-29124606 336055 Dunham, I. et.al. Plus 29166352-29166573 336072 Dunham, I. et.al. Plus 29269409-29269575 336075 Dunham, I. et.al. Plus 29343938-29344050 336081 Dunham, I. et.al. Plus 29372270-29372407 336083 Dunham, I. et.al. Plus 29379738-29379881 336084 Dunham, I. et.al. Plus 29380664-29380792 336086 Dunham, I. et.al. Plus 29385594-29385713 336087 Dunham, I. et.al. Plus 29387122-29387253 336088 Dunham, I. et.al. Plus 29389001-29389124 336089 Dunham, I. et.al. Plus 29401421-29401625 336090 Dunham, I. et.al. Plus 29413020-29413162 336091 Dunham, I. et.al. Plus 29415486-29415617 336092 Dunham, I. et.al. Plus 29438816-29438948 336094 Dunham, I. et.al. Plus 29567934-29568099 336102 Dunham, I. et.al. Plus 29681500-29681687 336124 Dunham, I. et.al. Plus 30053441-30053500 336125 Dunham, I. et.al. Plus 30056541-30056622 336127 Dunham, I. et.al. Plus 30058870-30059029 336128 Dunham, I. et.al. Plus 30059294-30059367 336171 Dunham, I. et.al. Plus 30223877-30224048 336214 Dunham, I. et.al. Plus 30561988-30562044 336306 Dunham, I. et.al. Plus 33172949-33173281 336316 Dunham, I. et.al. Plus 33338776-33338919 336333 Dunham, I. et.al. Plus 33673947-33677345 336387 Dunham, I. et.al. Plus 34013939-34014124 336442 Dunham, I. et.al. Plus 34187937-34188081 336481 Dunham, I. et.al. Plus 34231611-34231720 336489 Dunham, I. et.al. Plus 34239511-34239619 336498 Dunham, I. et.al. Plus 34267340-34267424 336502 Dunham, I. et.al. Plus 34268953-34269083 336516 Dunham, I. et.al. Plus 34296068-34296249 336548 Dunham, I. et.al. 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Minus 5683253-5683016 336854 Dunham, I. et.al. Minus 7884839-7884767 336858 Dunham, I. et.al. Minus 8200946-8200789 336882 Dunham, I. et.al. Minus 8394593-8394369 336863 Dunham, I. et.al. Minus 8396673-8396425 336883 Dunham, I. et.al. Minus 9322767-9322554 336908 Dunham, I. et.al. Minus 10791347-10791256 336927 Dunham, I. et.al. Minus 11548111-11547937 336929 Dunham, I. et.al. Minus 11603040-11602908 336978 Dunham, I. et.al. Minus 14241223-14241030 336981 Dunham, I. et.al. Minus 14478638-14478472 336984 Dunham, I. et.al. Minus 14725450-14725309 336994 Dunham, I. et.al. Minus 15104752-15104656 336999 Dunham, I. et.al. Minus 15389579-15388897 337011 Dunham, I. et.al. Minus 16106423-16106080 337023 Dunham, I. et.al. Minus 16346174-16346065 337069 Dunham, I. et.al. Minus 19014379-19014222 337092 Dunham, I. et.al. Minus 20140132-20139980 337093 Dunham, I. et.al. Minus 20145693-20145570 337094 Dunham, I. et.al. Minus 20146915-20146778 337097 Dunham, I. et.al. Minus 20498648-20497686 337100 Dunham, I. et.al. Minus 20543630-20543751 337114 Dunham, I. et.al. Minus 21328259-21328050 337203 Dunham, I. et.al. Minus 25349286-25349156 337204 Dunham, I. et.al. Minus 25419024-25418931 337225 Dunham, I. et.al. Minus 26607638-26607468 337244 Dunham, I. et.al. Minus 27362048-27361952 337279 Dunham, I. et.al. Minus 28430185-28430033 337289 Dunham, I. et.al. Minus 28756246-28756163 337316 Dunham, I. et.al. Minus 29657129-29656997 337431 Dunham, I. et.al. Minus 32110529-32110475 337432 Dunham, I. et.al. Minus 32199134-32198922 337445 Dunham, I. et.al. Minus 32292380-32292228 337451 Dunham, I. et.al. Minus 32408680-32408576 337452 Dunham, I. et.al. Minus 32415187-32415117 337455 Dunham, I. et.al. Minus 32434517-32434425 337456 Dunham, I. et.al. Minus 32438887-32438828 337513 Dunham, I. et.al. Minus 33478692-33478562 337514 Dunham, I. et.al. Minus 33484408-33484339 337517 Dunham, I. et.al. Minus 33795568-33795385 337590 Dunham, I. et.al. Minus 982397-982246 337592 Dunham, I. et.al. Minus 1007791-1007634 337604 Dunham, I. et.al. Minus 1329838-1329759 337606 Dunham, I. et.al. Minus 1346786-1346617 337612 Dunham, I. et.al. Minus 1570235-1570142 337645 Dunham, I. et.al. Minus 5141462-5141329 337704 Dunham, I. et.al. Minus 3658670-3658545 337706 Dunham, I. et.al. Minus 3672056-3671922 337760 Dunham, I. et.al. Minus 4008389-4008037 337768 Dunham, I. et.al. Minus 4050134-4049973 337771 Dunham, I. et.al. Minus 4060797-4060707 337778 Dunham, I. et.al. Minus 4087301-4087157 337787 Dunham, I. et.al. Minus 4135097-4135025 337816 Dunham, I. et.al. Minus 4523203-4523090 337821 Dunham, I. et.al. Minus 4538189-4538075 337848 Dunham, I. et.al. Minus 5053964-5053829 337911 Dunham, I. et.al. Minus 5866504-5866154 337913 Dunham, I. et.al. Minus 6149843-6149786 337974 Dunham, I. et.al. Minus 7153401-7153085 337984 Dunham, I. et.al. Minus 7282160-7282020 338069 Dunham, I. et.al. Minus 8728655-8728580 338087 Dunham, I. et.al. Minus 9362067-9361878 338113 Dunham, I. et.al. Minus 10481242-10481089 338132 Dunham, I. et.al. Minus 10989617-10989530 338140 Dunham, I. et.al. Minus 11237977-11237876 338151 Dunham, I. et.al. Minus 11519629-11519501 338221 Dunham, I. et.al. Minus 14183649-14183568 338223 Dunham, I. et.al. Minus 14287001-14286830 338235 Dunham, I. et.al. Minus 14484254-14484179 338271 Dunham, I. et.al. Minus 16048151-16047985 338285 Dunham, I. et.al. Minus 16276030-16274895 338306 Dunham, I. et.al. Minus 16966519-16966247 338325 Dunham, I. et.al. Minus 17241596-17241507 338368 Dunham, I. et.al. Minus 18272087-18272025 338381 Dunham, I. et.al. Minus 18534404-18534234 338431 Dunham, I. et.al. Minus 19747608-19747496 338450 Dunham, I. et.al. Minus 20172384-20172200 338451 Dunham, I. et.al. Minus 20174286-20174193 338486 Dunham, I. et.al. Minus 21063152-21063049 338508 Dunham, I. et.al. Minus 21308161-21307923 338576 Dunham, I. et.al. Minus 22676619-22676368 338591 Dunham, I. et.al. Minus 22959271-22959182 338593 Dunham, I. et.al. Minus 22992718-22992531 338594 Dunham, I. et.al. Minus 23026144-23026029 338668 Dunham, I. et.al. Minus 24500606-24500442 338686 Dunham, I. et.al. Minus 24836463-24838246 338725 Dunham, I. et.al. Minus 25904148-25904017 338819 Dunham, I. et.al. Minus 27539222-27539058 338829 Dunham, I. et.al. Minus 27739328-27739163 338843 Dunham, I. et.al. Minus 27899321-27899045 338934 Dunham, I. et.al. Minus 29036147-29036048 338976 Dunham, I. et.al. Minus 29867484-29867259 338990 Dunham, I. et.al. Minus 30019967-30019837 339019 Dunham, I. et.al. Minus 30498278-30498118 339032 Dunham, I. et.al. Minus 30613407-30613275 339033 Dunham, I. et.al. Minus 30621102-30620830 339037 Dunham, I. et.al. Minus 30634104-30633988 339044 Dunham, I. et.al. Minus 30721853-30721740 339071 Dunham, I. et.al. Minus 30885702-30885511 339127 Dunham, I. et.al. Minus 31688232-31688072 339130 Dunham, I. et.al. Minus 31743961-31743767 339181 Dunham, I. et.al. Minus 32321697-32321571 339188 Dunham, I. et.al. Minus 32347554-32347250 339193 Dunham, I. et.al. Minus 32415060-32414928 339196 Dunham, I. et.al. Minus 32431422-32431097 339208 Dunham, I. et.al. Minus 32491714-32491657 339213 Dunham, I. et.al. Minus 32496590-32496440 339215 Dunham, I. et.al. Minus 32502559-32502383 339220 Dunham, I. et.al. Minus 32519184-32519081 339230 Dunham, I. et.al. Minus 32729004-32728929 339251 Dunham, I. et.al. Minus 32894314-32894216 339256 Dunham, I. et.al. Minus 32926055-32925967 339266 Dunham, I. et.al. Minus 32976148-32976041 339288 Dunham, I. et.al. Minus 32984700-32984500 339280 Dunham, I. et.al. Minus 33114230-33114010 339340 Dunham, I. et.al. Minus 33485220-33485144 339342 Dunham, I. et.al. Minus 33494677-33494541 339344 Dunham, I. et.al. Minus 33503675-33503520 339363 Dunham, I. et.al. Minus 33589964-33589665 339365 Dunham, I. et.al. Minus 33641615-33641446 339401 Dunham, I. et.al. Minus 34045393-34045138 339424 Dunham, I. et.al. Minus 34392464-34392311 339435 Dunham, I. et.al. Minus 34538987-34538876 337884 337885 337895 337898 329611 3962478 Minus 11780-11875 329496 3983518 Plus 13570-13686 325310 5866864 Minus 17256-17357 325320 5866670 Minus 33200-33646 325338 5666883 Minus 62747-62928 325271 5866901 Plus 87318-87378 325285 5866903 Plus 107772-107864 325289 5866903 Minus 129715-129877 325300 5866908 Minus 7940-8059 325304 5866910 Minus 37466-37884 329630 6729060 Minus 167326-167511 325369 5866920 Minus 1018736-1018830 325359 5866920 Plus 392668-392781 325408 5866921 Plus 599118-599289 325409 5866921 Plus 599438-599655 325410 5866921 Plus 615477-615580 325393 5866921 Minus 350513-350691 325396 5866921 Plus 476868-477200 325433 5866936 Minus 480706-480826 325448 5866941 Minus 392834-392982 325464 5866947 Plus 323995-324279 325480 5866957 Plus 20558-21112 325482 5866957 Plus 47957-48078 325510 5866974 Plus 219958-220917 325524 5866981 Minus 117837-117997 325513 6017035 Minus 34295-34490 325519 6017036 Minus 186804-186915 325571 6552439 Minus 184952-185135 329638 3779004 Minus 4636-5127 325623 5867000 Plus 84366-84472 325636 5867002 Minus 149928-150033 325677 5867017 Minus 58414-58518 325691 5867021 Plus 65467-65629 325690 5867021 Plus 7391-7530 325702 5867028 Plus 139925-140061 325703 5867028 Plus 155806-156098 325790 6381957 Minus 105385-105524 325783 6456780 Plus 102815-102957 325695 6552446 Minus 199599-199778 325726 6552447 Plus 154262-154623 325742 6552448 Minus 38225-38306 325760 6552449 Plus 343394-343549 325801 6552451 Plus 49269-49542 325803 6552451 Plus 53355-53558 325649 6588011 Minus 215659-215815 325710 6682473 Plus 204538-204822 325712 6682473 Plus 208541-208926 325755 6682474 Plus 406603-407037 325751 6682474 Plus 130437-130520 325763 6682475 Minus 327530-327910 325791 6682476 Plus 344059-344841 329782 5912597 Plus 123410-123499 329779 6002090 Minus 195353-195669 329760 6048280 Minus 51419-51528 329752 6065777 Plus 132916-133335 329737 6065779 Plus 70136-70236 329735 6065780 Plus 63923-64213 329719 6065785 Plus 46970-47762 329725 6065785 Plus 133747-133842 329705 6065790 Minus 63183-63724 329665 6272129 Plus 91791-91891 329793 6522661 Minus 96556-96698 329824 6630758 Minus 126072-126254 329839 6672062 Plus 34377-34537 329853 6682295 Plus 68945-69009 329870 6706435 Minus 5729-5870 329879 6466518 Minus 12266-12356 329902 6634760 Plus 106906-106984 325851 5867067 Minus 51751-51981 325886 5867087 Plus 194694-194915 325887 5867087 Plus 195052-195485 326005 5867112 Minus 7827-8117 325945 5867138 Minus 123079-124086 325953 5867140 Minus 4721-4901 325965 5867147 Plus 216364-216516 325966 5867147 Plus 217235-217356 325977 6249602 Plus 60638-60759 325835 6552452 Minus 81182-81414 329995 4567166 Minus 150014-150315 329948 5540101 Minus 134056-134261 329940 6165199 Minus 33718-33882 329921 6165205 Minus 33759-33891 330002 6623963 Plus 46097-46158 330021 6671889 Plus 120938-121032 326162 5867168 Minus 5870-6291 326070 5867175 Plus 132181-132731 326029 5867176 Minus 112558-112669 326033 5867178 Plus 37261-37333 326039 5867179 Minus 15157-15227 326122 5867194 Plus 144397-144683 326136 5867202 Minus 155973-156065 326194 5867213 Plus 75271-75522 326206 5867219 Plus 113881-115080 326218 5867226 Minus 259784-259920 326224 5867230 Plus 21528-21667 326240 5867260 Plus 94843-96127 326253 5867263 Minus 222216-222341 326249 5867263 Minus 80253-80323 326266 5867264 Plus 337993-338192 326304 5867277 Minus 367450-367559 326309 5867277 Plus 614150-614294 326310 5867277 Plus 621555-621698 326338 6056311 Minus 161972-162333 326343 6525295 Minus 2699-2777 326344 6525295 Minus 3207-3365 326073 6682495 Minus 248865-249009 330057 6478962 Plus 75145-75287 330058 6634847 Plus 100602-100963 330061 6721261 Plus 4254-4388 326539 5867307 Plus 198357-198504 326545 5867307 Plus 600850-601425 326549 5867307 Plus 698004-698069 326552 5867308 Minus 6988-7107 326554 5867308 Plus 16259-18271 326559 5867310 Plus 159233-159439 326577 5867317 Plus 215987-216127 326380 5867327 Plus 32474-32668 326412 5867362 Minus 9263-9436 326417 5867362 Plus 89132-89383 326418 5867365 Plus 23609-23745 326423 5867369 Minus 142311-142500 326458 5867400 Plus 128045-128147 326459 5867400 Plus 137590-138212 326506 5867435 Minus 9368-9509 326509 6682496 Plus 92406-92680 330112 6015238 Plus 32059-32163 330086 6015293 Plus 29518-29662 330080 6015314 Minus 4890-4972 330082 6015314 Plus 27158-27296 330064 6165044 Minus 5619-5696 330063 6165044 Minus  948-1025 330065 6165044 Minus 9876-9948 326646 5867562 Plus 100426-100608 326688 5867582 Plus 104875-105531 326708 5867593 Minus 39203-39310 326710 5867593 Minus 80204-80468 326746 5867611 Plus 129366-129565 326793 5867631 Plus 136295-136518 326603 6056312 Minus 50323-50575 326806 6469835 Plus 101628-102149 326783 6525298 Plus 196378-196863 326668 6552455 Plus 146726-146838 326725 6552456 Minus 223005-223125 326857 6552460 Minus 120142-120345 326763 6598307 Plus 239690-239902 326808 6682504 Minus 65107-65214 326874 6682507 Minus 4643-4888 326876 6682507 Minus 46203-46499 326884 6682511 Plus 33403-33479 326997 5867660 Minus 71389-72147 327009 5867654 Plus 933145-933266 327015 5867664 Plus 1030457-1030534 326942 6004446 Minus 88675-88785 326943 6004446 Minus 89242-89427 326957 6469836 Plus 37529-37694 327049 6531965 Minus 1924026-1924110 327051 6531965 Plus 2222592-2222717 327056 6531965 Plus 2374323-2374751 327059 6531965 Plus 2421032-2421799 327067 6531965 Minus 3726023-3726668 327089 6531965 Plus 5238983-5239187 327037 6531965 Minus 387854-388045 327123 6531971 Minus 23980-24340 327125 6531971 Plus 48884-48975 326981 6588016 Plus 105091-106038 330139 4210430 Plus 112089-112450 330153 4325335 Plus 146951-147475 330130 6002196 Minus 241903-241967 327203 5867447 Plus 36485-36577 327206 5867447 Plus 177855-178031 327259 5867454 Plus 87268-87438 327264 5867461 Plus 47014-47367 327273 5867466 Plus 73451-73549 327274 5867470 Minus 84027-84128 327277 5867473 Minus 165616-165715 327278 5867473 Minus 166350-166439 327289 5867481 Plus 49296-49536 327304 5867494 Plus 20664-20850 327315 5867508 Minus 78409-79245 327246 5867547 Plus 136212-136325 327155 5867549 Plus 90343-90876 327159 5867550 Minus 8219-8331 327334 5902477 Minus 142655-142745 327341 6017016 Minus 122906-123014 327185 6117805 Minus 3287-3451 327309 6456757 Minus 10219-10457 327263 6525274 Minus 153814-154920 327362 6552412 Minus 62459-62805 327413 5867750 Plus 101410-101508 327418 5867750 Minus 153453-153547 327430 5867754 Plus 1320-1403 327431 5867754 Plus 1853-1958 327472 5867775 Plus 74628-74937 327487 5867785 Minus 146220-146326 327379 5867795 Plus 1368-1820 327461 6004455 Plus 209031-209210 327532 6469818 Plus 71994-72137 330170 6648220 Plus 103280-103849 330166 6648220 Plus 86542-86867 327544 5867797 Minus 18105-18332 327564 5867811 Plus 13850-14018 327566 5867811 Plus 33383-33901 327581 5867825 Plus 5318-5434 327585 5867825 Plus 85660-85764 327605 6004463 Plus 199214-199579 327710 5867860 Minus 131012-131790 327610 5867868 Minus 174109-174278 327624 5867871 Minus 37699-37788 327641 5867890 Plus 13583-13702 327646 5867894 Minus 3043-3258 327614 6525283 Plus 3634-4001 327736 5867940 Minus 37781-37887 327739 5867942 Minus 182187-182548 327740 5867943 Plus 25716-26077 327743 5867944 Minus 155930-156098 327755 5867955 Minus 61969-62145 327772 5867964 Minus 26185-26285 327774 5867964 Minus 127659-127899 327823 5867968 Minus 170359-170433 327827 5867968 Minus 201918-202048 327833 5867968 Minus 303618-303732 327805 5867968 Plus 19952-20019 327809 5867968 Plus 54610-54761 327816 5867968 Minus 79202-79552 327790 5867977 Plus 19822-19985 327791 5867977 Plus 22491-22610 327793 5867979 Plus 18874-19254 327845 6531962 Plus 193402-193549 327846 6531962 Plus 195216-195373 330204 6013606 Plus 86663-86811 330189 6165182 Minus 26732-26991 330239 6671857 Plus 117484-118092 330266 6671885 Minus 129505-129832 330275 6671904 Plus 103585-103716 330280 6671910 Plus 2109-2377 330286 6671913 Minus 31050-31171 327999 5867994 Plus 94710-94841 328109 5868020 Minus 353895-354525 328098 5868020 Minus 261745-261920 328134 5868039 Plus 72354-72487 328171 5868071 Plus 101102-101224 328221 5868099 Minus 37489-37829 328224 5868101 Plus 105563-105832 328228 5868105 Minus 21488-21596 328236 5868117 Plus 13864-14371 327864 5868130 Plus 59139-59358 327888 5868149 Minus 51964-52120 327899 5868156 Minus 102288-102697 327925 5868172 Minus 118396-118490 327927 5868173 Plus 50989-51246 327937 5868192 Minus 33127-33485 327946 5868206 Plus 44102-44319 327982 5868216 Plus 30307-30527 327990 5868218 Minus 36225-36503 328015 5902482 Minus 477679-478113 328016 5902482 Minus 507572-508519 328025 5902482 Minus 931937-932171 328031 5902482 Plus 1176372-1177283 328053 5902482 Minus 2709850-2710010 328243 6056292 Plus  1-243 328271 6552415 Plus 39015-39098 328592 5868227 Minus 252407-252565 328570 5868231 Plus 89210-89816 328607 5868233 Minus 246798-246944 328620 5868241 Minus 15651-15788 328624 5868246 Minus 120666-120836 328791 5868309 Plus 171592-171929 328810 5868327 Plus 101730-101914 328820 5868330 Plus 90446-90602 328835 5868339 Plus 88053-88461 328282 5868353 Plus 72692-72819 328314 5868371 Minus 288397-288505 328328 5868375 Plus 169210-169407 328420 5868411 Plus 53612-53886 328428 5868417 Plus 13599-13780 328436 5868417 Plus 203760-203904 328444 5868420 Plus 65393-66103 328462 5868433 Plus 49649-49768 328467 5868434 Minus 15954-16073 328474 5868446 Minus 128777-128970 328484 5868454 Minus 21974-22140 328504 5868471 Plus 47064-47217 328506 5868471 Plus 60716-60830 328507 5868473 Minus 199637-199990 328544 5868486 Plus 145659-145829 328552 5868489 Plus 47328-47607 328557 5868489 Plus 138094-138161 328558 5868489 Plus 143648-144108 328276 6004471 Plus 13282-13450 328277 6004471 Minus 279901-280181 328662 6004473 Plus 1184773-1184855 328636 6004473 Plus 192484-192543 328803 6004475 Minus 291716-291948 328305 6004478 Minus 34730-34851 328569 6004480 Plus 232896-233243 328581 6006033 Minus 121249-121400 328582 6006033 Minus 134177-134282 328768 6017031 Minus 223741-224238 328770 6017031 Minus 363933-364166 328841 6381920 Minus 5214-5479 328851 6381923 Plus 2502-2606 328859 6381928 Plus 69045-69138 328860 6381928 Plus 83265-83366 328863 6381929 Minus 29313-29506 328868 6381930 Plus 112825-112993 328876 6525286 Plus 94053-94185 328886 6588003 Plus 31068-31429 328888 6588003 Minus 111901-111999 328936 5868500 Minus 1352202-1352259 328938 5868500 Plus 1522923-1522986 328971 6478806 Minus 23976-24105 330338 5457162 Plus 48406-48518 330327 5919194 Plus 121561-121683 330319 5932415 Plus 49095-50132 328974 5868520 Plus 31557-31668 328981 5868527 Minus 105677-105764 328989 5868535 Plus 182088-182198 330363 3126882 Minus 61838-61901 330370 6580495 Plus 10826-11669 329041 5868564 Plus 141592-141785 329078 5868597 Plus 326798-326860 329097 5868624 Plus 12002-12170 329107 5868626 Plus 101063-101190 329114 5868650 Minus 23792-23910 329116 5868650 Minus 43389-43493 329164 5868691 Plus 62305-62517 329187 5868713 Plus 29909-30175 329201 5868718 Plus 79266-79539 329221 5868727 Minus 105837-105894 329246 5868732 Minus 250541-250792 329254 5868733 Plus 4133-4214 329326 5868806 Plus 155884-155992 329330 5868806 Minus 340278-340403 329382 5868868 Plus 41401-41655 329384 5868869 Minus 116524-116662 329386 6004484 Plus 160502-161110 329140 6017060 Plus 290842-290905 329182 6056331 Minus 662206-663423 329018 6249620 Plus 103950-104034 329319 6381976 Plus 721390-721470 329392 6478815 Plus 109786-109854 329029 6525302 Plus 281445-282490 329401 6682544 Plus 21342-24014 329406 6682547 Plus 47249-47395 329411 6682549 Minus 84558-84835 329429 5868882 Minus 97008-97091 329436 5868883 Plus 230265-230528 329464 6456788 Minus 4437-4538 #genomic sequence source used for prediction. Nucleotide locations of each predicted exon are also listed.

[0349] TABLE 21 310 GENES UP-REGULATED IN COLON CANCER DERIVED LIVER METASTASES COMPARED TO NORMAL COLON TISSUE Pkey ExAccn UnigeneID Unigene Title R1 446619 AU076643 Hs.313 secreted phosphoprotein 1 (osteopontin, 26.72 431958 X63629 Hs.2877 cadherin 3, type 1, P-cadherin (placenta 16.36 409041 AB033025 Hs.50081 KIAA1199 protein 13.94 444381 BE387335 Hs.283713 ESTs, Weakly similar to S64054 hypotheti 13.90 432314 AA533447 Hs.312989 ESTs 12.24 428330 L22524 Hs.2256 matrix metalloproteinase 7 (matrilysin, 11.60 443162 T49951 Hs.9029 DKFZP434G032 protein 9.52 436385 BE551618 Hs.144097 ESTs 9.20 418662 AI801098 Hs.151500 ESTs 9.00 433312 AI241331 Hs.131765 ESTs, Moderately similar to I38937 DNA/R 8.90 412093 BE242691 Hs.14947 ESTs 8.74 442369 AI565071 Hs.159983 ESTs 8.40 426101 AL049987 Hs.166361 Homo sapiens mRNA; cDNA DKFZp564F112 (fr 8.39 435937 AA830893 Hs.119769 ESTs 8.22 452281 T93500 Hs.28792 Homo sapiens cDNA FLJ11041 fis, clone PL 8.22 432572 AI660840 Hs.191202 ESTs, Weakly similar to ALUE_HUMAN !!!! 7.96 440524 R71264 Hs.16798 ESTs 7.94 424878 H57111 Hs.221132 ESTs 7.88 430433 AA478883 Hs.273766 ESTs 7.82 410245 C17908 Hs.194125 ESTs 7.78 417315 AI080042 Hs.336901 ribosomal protein S24 7.76 430665 BE350122 Hs.157367 ESTs, Weakly similar to I78885 serine/th 7.76 432435 BE218886 Hs.282070 ESTs 7.74 426818 AA554827 Hs.289115 DKFZp434A0131 protein 7.58 419145 N99638 gb: za39g11.r1 Soares fetal liver spleen 7.56 444838 AV651680 Hs.208558 ESTs 7.54 428046 AW812795 Hs.155381 ESTs, Moderately similar to I38022 hypot 7.48 446682 AW205632 Hs.211198 ESTs 7.26 421221 AW276914 Hs.326714 Homo sapiens clone IMAGE: 713177, mRNA se 7.19 440116 AI798851 Hs.283108 hemoglobin, gamma G 7.12 450230 AW016607 Hs.201582 ESTs 7.08 456332 AA228357 gb: nc39d05.r1 NCI_CGAP_Pr2 Homo sapiens 7.04 421814 L12350 Hs.108623 thrombospondin 2 6.89 440774 AI420611 Hs.127832 ESTs 6.86 428065 AI634046 Hs.157313 ESTs 6.78 422330 D30783 Hs.115263 epiregulin 6.72 413950 AA249096 Hs.32793 ESTs 6.67 438011 BE466173 Hs.145696 splicing factor (CC1.3) 6.62 421057 T58283 Hs.10450 Homo sapiens cDNA: FLJ22063 fis, clone H 6.58 428698 AA852773 Hs.334838 KIAA1866 protein 6.40 408806 AW847814 Hs.289005 Homo sapiens cDNA: FLJ21532 fis, clone C 6.38 425787 AA363867 Hs.155029 ESTs 6.38 435812 AA700439 Hs.188490 ESTs 6.32 448974 AL049390 Hs.22689 Homo sapiens mRNA; cDNA DKFZp586O1318 (f 6.28 418875 W19971 Hs.233459 ESTs 6.22 407284 AI539227 Hs.214039 hypothetical protein FLJ23556 6.17 408243 Y00787 Hs.624 interleukin 8 6.12 434936 AI285970 Hs.183817 ESTs 6.12 412088 AI689496 Hs.108932 ESTs 6.04 450377 AB033091 Hs.74313 KIAA1265 protein 6.00 407618 AW054922 Hs.53478 Homo sapiens cDNA FLJ12366 fis, clone MA 5.98 408296 AL117452 Hs.44155 DKFZP586G1517 protein 5.94 456999 AA319798 Hs.298581 eukaryotic translation elongation factor 5.90 432559 AW452948 Hs.257631 ESTs 5.88 423349 AF010258 Hs.127428 homeo box A9 5.84 436100 AA704806 Hs.143842 ESTs, Weakly similar to 2004399A chromos 5.84 453204 R10799 Hs.191990 ESTs 5.84 429183 AB014604 Hs.197955 KIAA0704 protein 5.78 427882 AA640987 Hs.193767 ESTs 5.72 447033 AI357412 Hs.157601 ESTs 5.70 428054 AI948688 Hs.266619 ESTs 5.66 414504 AW069181 Hs.115175 sterile-alpha motif and leucine zipper c 5.64 442806 AW294522 Hs.149991 ESTs 5.64 418259 AA215404 Hs.137289 ESTs 5.60 434963 AW974957 Hs.288719 Homo sapiens cDNA FLJ12142 fis, clone MA 5.60 419999 AI760942 Hs.191754 ESTs 5.58 431749 AL049263 Hs.306292 Homo sapiens mRNA; cDNA DKFZp564F133 (fr 5.58 422790 AA809875 Hs.25933 ESTs 5.56 440980 AL042005 Hs.1117 tripeptidyl peptidase II 5.48 432451 AW972771 Hs.292471 ESTs, Weakly similar to ALU1_HUMAN ALU S 5.46 438578 AA811244 Hs.164168 ESTs 5.44 410467 AF102546 Hs.63931 dachshund (Drosophila) homolog 5.42 426317 AA312350 Hs.169294 transcription factor 7 (T-cell specific, 5.42 450164 AI239923 Hs.30098 ESTs 5.40 438899 AF085833 Hs.135624 ESTs 5.38 432945 AL043683 Hs.8173 hypothetical protein FLJ10803 5.36 437176 AW176909 Hs.42346 calcineurin-binding protein calsarcin-1 5.34 419829 AI924228 Hs.115185 ESTs, Moderately similar to PC4259 ferri 5.33 407966 AA295052 Hs.38516 Homo sapiens, clone MGC:15887, mRNA, com 5.30 447342 AI199268 Hs.19322 Homo sapiens, Similar to RIKEN cDNA 2010 5.26 419682 H13139 Hs.92282 paired-like homeodomain transcription fa 5.26 421097 AI280112 Hs.125232 Homo sapiens cDNA FLJ13266 fis, clone OV 5.22 443373 AI792868 Hs.135365 ESTs 5.22 412059 AA317962 Hs.249721 ESTs, Moderately similar to PC4259 ferri 5.21 443651 W22152 Hs.282929 ESTs 5.21 411274 NM_002776 Hs.69423 kallikrein 10 5.17 421999 U50535 Hs.110630 Human BRCA2 region, mRNA sequence CG006 5.17 426981 AL044675 Hs.173081 KIAA0530 protein 5.14 431319 AA873350 Hs.302232 ESTs 5.10 434966 AA657494 gb: nt66f04.s1 NCI_CGAP_Pr3 Homo sapiens 5.10 418830 BE513731 Hs.88959 hypothetical protein MGC4816 5.08 428290 AI932995 Hs.183475 Homo sapiens clone 25061 mRNA sequence 5.07 408784 AW971350 Hs.63386 ESTs 5.04 411975 AI916058 Hs.144583 ESTs 5.02 409760 AA302840 gb: EST10534 Adipose tissue, white I Homo 4.97 420717 AA284447 Hs.271887 ESTs 4.96 417035 AA192455 Hs.22968 Homo sapiens clone IMAGE: 451939, mRNA se 4.95 434442 AA737415 Hs.152826 ESTs 4.94 441328 AI982794 Hs.159473 ESTs 4.92 438962 BE046594 gb: hn41c11.x1 NCI_CGAP_RDF2 Homo sapiens 4.92 451277 AK001123 Hs.26176 hypothetical protein FLJ10261 4.92 438406 BE273296 Hs.254467 Homo sapiens cDNA FLJ13255 fis, clone OV 4.90 424950 AA602917 Hs.156974 ESTs 4.88 436823 AW749865 Hs.293645 ESTs, Weakly similar to I38022 hypotheti 4.87 444783 AK001468 Hs.62180 anillin (Drosophila Scraps homolog), act 4.82 444301 AK000136 Hs.10760 asporin (LRR dass 1) 4.80 445390 AI222165 Hs.144923 ESTs 4.80 439608 AW864696 Hs.301732 hypothetical protein MGC5306 4.78 450506 NM_004460 Hs.418 fibroblast activation protein, alpha 4.78 432682 AI376400 Hs.159588 ESTs 4.76 426086 T94907 Hs.188572 ESTs 4.76 435981 H74319 Hs.188620 ESTs 4.74 432340 AA534222 gb: nj21d02.s1 NCI_CGAP_AA1 Homo sapiens 4.72 435756 AI418466 Hs.33665 ESTs 4.72 447982 H22953 Hs.137551 ESTs 4.72 449509 AA001615 Hs.84561 ESTs 4.72 407946 AA226495 Hs.154292 ESTs 4.70 426215 AW963419 Hs.155223 stanniocalcin 2 4.70 414783 AW069569 Hs.278270 unactive progesterone receptor, 23 kD 4.68 417601 NM_014735 Hs.82292 KIAA0215 gene product 4.68 438401 AW075485 Hs.286049 phosphoserine aminotransferase 4.68 449032 AA045573 Hs.22900 nuclear factor (erythroid-derived 2)-lik 4.68 426501 AW043782 Hs.293616 ESTs 4.67 409024 AW883529 Hs.173830 ESTs, Weakly similar to ALU7_HUMAN ALU S 4.67 439848 AW979249 gb: EST391359 MAGE resequences, MAGP Homo 4.66 424762 AL119442 Hs.183684 eukaryotic translation initiation factor 4.66 442007 AA301116 Hs.142838 nucleolar phosphoprotein Nopp34 4.62 409632 W74001 Hs.55279 serine (or cysteine) proteinase inhibito 4.62 432409 AA806538 Hs.130732 KIAA1575 protein 4.60 452220 BE158006 Hs.212296 ESTs 4.60 442577 AA292998 Hs.163900 ESTs 4.58 434001 AW950905 Hs.3697 serine (or cysteine) proteinase inhibito 4.58 414271 AK000275 Hs.75871 protein kinase C binding protein 1 4.58 433854 AA610649 Hs.333239 ESTs 4.56 431315 AW972227 Hs.163986 Homo sapiens cDNA: FLJ22765 fis, clone K 4.53 434220 AI174777 Hs.283039 Homo sapiens PRO2492 mRNA, complete cds 4.50 457752 AI821270 Hs.285643 Homo sapiens cDNA FLJ14364 fis, clone HE 4.50 449941 AW450536 Hs.209260 ESTs 4.48 415116 AA160363 Hs.269956 ESTs 4.47 414386 X00442 Hs.75990 haptoglobin 4.47 422956 BE545072 Hs.122579 hypothetical protein FLJ10461 4.44 423974 AL118754 gb: DKFZp761P1910_r1 761 (synonym: hamy2) 4.44 449618 AI076459 Hs.15978 KIAA1272 protein 4.44 428279 AA425310 Hs.155768 ESTs, Weakly similar to A47582 B-4 cell gr 4.42 430573 AA744550 Hs.136345 ESTs 4.42 430929 AA489166 Hs.156933 ESTs 4.40 433530 BE349534 Hs.281789 ESTs 4.40 446099 T93096 Hs.17126 hypothetical protein MGC15912 4.40 447082 T85314 Hs.42644 thioredoxin-like 4.39 407168 R45175 Hs.117183 ESTs 4.38 417067 AJ001417 Hs.81086 solute carrier family 22 (extraneuronal 4.38 408380 AF123050 Hs.44532 diubiquitin 4.36 431379 AA504264 Hs.182937 peptidylprolyl isomerase A (cyclophilin 4.36 406671 AA129547 Hs.285754 met proto-oncogene (hepatocyte growth fa 4.34 419317 AA236282 Hs.172318 ESTs 4.32 450295 AI766732 Hs.210628 ESTs 4.32 423578 AW960454 Hs.222830 ESTs 4.31 419553 N34145 Hs.250614 ESTs, Moderately similar to ZN91_HUMAN Z 4.31 429512 AA453987 Hs.144802 ESTs 4.30 426848 H72531 Hs.36190 ESTs 4.30 429831 AA564489 Hs.137526 ESTs 4.30 433735 AA608955 Hs.109653 ESTs 4.30 450546 AA010200 Hs.175551 ESTs 4.27 421059 AI654133 Hs.30212 thyroid receptor interacting protein 15 4.27 413243 AA769266 Hs.193657 ESTs 4.26 433230 AW136134 Hs.220277 ESTs 4.22 439717 W94472 Hs.59529 ESTs, Moderately similar to ALU1_HUMAN A 4.20 439382 AI954880 Hs.134604 ESTs 4.19 450157 AW961576 Hs.60178 ESTs 4.17 451690 AW451469 Hs.209990 ESTs 4.17 418661 NM_001949 Hs.1189 E2F transcription factor 3 4.16 443135 AI376331 Hs.156103 ESTs 4.16 443148 AI034357 Hs.211194 ESTs, Weakly similar to ALU8_HUMAN ALU S 4.16 407765 AW076027 Hs.257711 ESTs, Moderately similar to ALU8_HUMAN A 4.14 428825 AI084336 Hs.128783 ESTs, Weakly similar to I38022 hypotheti 4.14 447519 U46258 Hs.339665 ESTs 4.14 439451 AF086270 Hs.278554 heterochromatin-like protein 1 4.12 450219 AI826999 Hs.224624 ESTs 4.12 431451 AA761378 Hs.192013 ESTs 4.11 432917 NM_014125 Hs.279812 PRO0327 protein 4.10 431328 AA502999 Hs.291591 ESTs 4.09 425992 AA367069 Hs.100636 ESTs 4.08 404571 4.06 420911 U77413 Hs.100293 O-linked N-acetylglucosamine (GlcNAc) tr 4.06 421114 AW975051 Hs.293156 ESTs, Weakly similar to I78885 serine/th 4.06 432731 R31178 Hs.287820 fibronectin 1 4.06 433588 AI056872 Hs.133386 ESTs 4.06 434658 AI624436 Hs.310286 ESTs 4.06 444040 AF204231 Hs.182982 golgin-67 4.06 444984 H15474 Hs.132898 fatty acid desaturase 1 4.06 438543 AA810141 Hs.192182 ESTs 4.05 413497 BE177661 gb: RC1-HT0598-020300-011-h02 HT0598 Homo 4.04 434575 AI133446 Hs.299964 Homo sapiens clone FLB7723 PRO2055 mRNA, 4.04 430256 AA470152 Hs.192195 ESTs 4.04 424839 AA740632 Hs.120850 ESTs, Weakly similar to ALU1_HUMAN ALU S 4.02 429048 AI372949 Hs.44241 Homo sapiens cDNA: FLJ21447 fis, clone C 4.02 449429 AA054224 Hs.59847 ESTs 4.02 410762 AF226053 Hs.66170 HSKM-B protein 4.00 418876 AA740616 gb: nyg7f11.s1 NCI_CGAP_GCB1 Homo sapiens 4.00 425905 AB032959 Hs.318584 novel C3HC4 type Zinc finger (ring finge 4.00 429500 X78565 Hs.289114 hexabrachion (tenascin C, cytotactin) 4.00 431393 AW971493 Hs.134269 ESTs, Highly similar to cytokine recepto 4.00 435008 AF150262 Hs.162898 ESTs 4.00 431361 AW971375 Hs.292921 ESTs 3.97 444816 Z48633 Hs.283742 H. sapiens, mRNA for retrotransposon 3.96 434701 AA460479 Hs.321707 KIAA0742 protein 3.96 413886 AW958264 Hs.103832 similar to yeast Upf3, variant B 3.95 424905 NM_002497 Hs.153704 NIMA (never in mitosis gene a)-related k 3.92 428479 Y00272 Hs.184572 cell division cycle 2, G1 to S and G2 to 3.91 435714 AA699325 Hs.269880 ESTs 3.86 447514 AI809314 Hs.208501 ESTs, Weakly similar to B34087 hypotheti 3.86 453818 BE256832 Hs.10711 hypothetical protein FLJ13449 3.85 433586 T85301 gb: yd78d06.s1 Soares fetal liver spleen 3.85 440638 AI376551 gb: te64e10.x1 Soares_NFL_T_GBC_S1 Homo s 3.85 417819 AI253112 Hs.133540 ESTs 3.84 409596 BE244200 Hs.55075 KIAA0410 gene product 3.83 423129 L44396 Hs.124106 Homo sapiens cDNA FLJ11941 fis, clone HE 3.83 453884 AA355925 Hs.36232 KIAA0186 gene product 3.83 431193 AW749505 Hs.296770 KIAA1719 protein 3.81 409262 AK000631 Hs.52256 hypothetical protein FLJ20624 3.80 425568 AW963118 Hs.161784 ESTs 3.78 441085 AW136551 Hs.181245 Homo sapiens cDNA FLJ12532 fis, clone NT 3.77 428079 AA421020 Hs.208919 ESTs 3.77 412490 AW803564 Hs.288850 Homo sapiens cDNA: FLJ22528 fis, clone H 3.76 435354 AA678267 Hs.117115 ESTs 3.75 436535 AW295687 Hs.254420 ESTs 3.74 420439 AW270041 Hs.193053 eukaryotic translation initiation factor 3.72 436090 AI640635 Hs.116468 EST 3.71 416265 AA177088 Hs.190065 ESTs 3.70 417715 AW969587 Hs.86366 ESTs 3.67 435677 AA694142 Hs.293726 ESTs, Weakly similar to TSGA RAT TESTIS 3.67 438607 AW080237 Hs.252884 ESTs 3.66 408194 AA601038 Hs.191797 ESTs, Weakly similar to S65657 alpha-1C- 3.65 417211 T97617 Hs.269092 ESTs 3.60 435538 AB011540 Hs.4930 low density lipoprotein receptor-related 3.59 410390 AA876905 Hs.125286 ESTs 3.58 438818 AW979008 Hs.222487 ESTs 3.57 431416 AA532718 Hs.178604 ESTs 3.57 433517 AW022133 Hs.189838 ESTs 3.56 428355 BE256452 Hs.2257 vitronectin (serum spreading factor, som 3.56 432954 AI076345 Hs.214199 ESTs 3.53 434466 AB037829 Hs.3862 regulator of nonsense transcripts 2; DKF 3.53 421933 R98881 Hs.109655 sex comb on midleg (Drosophila)-like 1 3.52 422082 AA016188 Hs.111244 hypothetical protein 3.52 437135 AL038624 Hs.208752 ESTs, Weakly similar to ALU8_HUMAN ALU S 3.49 424723 BE409813 Hs.152337 protein arginine N-methyltransferase 3(h 3.49 434280 BE005398 gb: CM1-BN0116-150400-189-h02 BN0116 Homo 3.49 407289 AA135159 Hs.203349 Homo sapiens cDNA FLJ12149 fis, clone MA 3.48 417670 R07785 gb: yf15c06.r1 Soares fetal liver spleen 3.48 431615 AW295859 Hs.235860 ESTs 3.48 429355 AW973253 Hs.292689 ESTs 3.45 430068 AA464964 gb: zx80f10.s1 Soares ovary tumor NbHOT H 3.45 432929 AW207166 Hs.191265 ESTs 3.44 437763 AA469369 Hs.5831 tissue inhibitor of metalloproteinase 1 3.44 445674 BE410347 Hs.13063 transcription factor CA150 3.42 408113 T82427 Hs.194101 Homo sapiens cDNA: FLJ20869 fis, clone A 3.42 408908 BE296227 Hs.250822 serine/threonine kinase 15 3.41 432235 AA531129 Hs.190297 ESTs 3.41 453985 N44545 Hs.251865 ESTs 3.41 415736 AA827082 Hs.291872 ESTs 3.38 430220 BE378277 Hs.152230 ESTs 3.37 426510 AW861225 Hs.194637 BANP homolog, SMAR1 homolog 3.37 412104 AW205197 Hs.240951 Homo sapiens, Similar to RIKEN cDNA 2210 3.36 411573 AB029000 Hs.70823 KIAA1077 protein 3.33 413816 AW958181 Hs.189998 ESTs 3.32 428057 AI343641 Hs.185798 ESTs 3.32 436280 AI690734 Hs.131740 Homo sapiens cDNA: FLJ22562 fis, clone H 3.31 449365 AW968261 Hs.118913 ESTs, Moderately similar to T46371 hypot 3.31 440659 AF134160 Hs.7327 claudin 1 3.30 436110 AA704899 Hs.291651 ESTs, Weakly similar to I38022 hypotheti 3.29 433862 D86960 Hs.3610 KIAA0205 gene product 3.29 424624 AB032947 Hs.151301 Ca2+ dependent activator protein for secr 3.29 439955 AW203959 Hs.149532 ESTs 3.28 417333 AL157545 Hs.42179 bromodomain and PHD finger containing, 3 3.28 436150 AW510927 Hs.125243 ESTs 3.27 414900 AW452420 Hs.248678 ESTs 3.26 439349 AI660898 Hs.195602 ESTs 3.25 428255 AI627478 Hs.187670 ESTs 3.24 436217 T53925 Hs.107 fibrinogen-like 1 3.24 429083 Y09397 Hs.227817 BCL2-related protein A1 3.24 422244 Y08890 Hs.113503 karyopherin (importin) beta 3 3.22 430178 AW449612 Hs.152475 ESTs 3.21 413810 AW197644 Hs.19107 ESTs 3.20 428728 NM_016625 Hs.191381 hypothetical protein 3.20 437151 AA745618 Hs.194637 BANP homolog, SMAR1 homolog 3.19 427051 BE178110 Hs.173374 Homo sapiens cDNA FLJ10500 fis, clone NT 3.19 438378 AW970529 Hs.86434 hypothetical protein FLJ21816 3.19 439943 AW083789 Hs.124620 ESTs 3.18 439280 AI125436 Hs.48752 ESTs 3.18 452336 AA960961 Hs.305953 zinc finger protein 83 (HPF1) 3.17 433713 AW976511 Hs.112592 ESTs 3.16 414998 NM_002543 Hs.77729 oxidised low density lipoprotein (lectin 3.14 407328 AA508857 Hs.187748 ESTs, Weakly similar to ALU1_HUMAN ALU S 3.14 432722 AA830532 Hs.326150 ESTs 3.14 419457 AA243146 Hs.209334 ESTs, Moderately similar to S23A_HUMAN P 3.11 449987 AW079749 Hs.184719 ESTs, Weakly similar to ALU1_HUMAN ALU S 3.11 418522 AA605038 Hs.7149 Homo sapiens cDNA: FLJ21950 fis, clone H 3.09 409969 AW514668 Hs.194258 ESTs, Moderately similar to ALU5_HUMAN A 3.08 436299 AK000767 Hs.5111 hypothetical protein FLJ20729 3.08 406687 M31126 Hs.272620 pregnancy specific beta-1-glycoprotein 9 3.07 408242 AA251594 Hs.43913 PIBF1 gene product 3.07 444614 R44284 Hs.2730 heterogeneous nuclear ribonucleoprotein 3.06 459407 N92114 gb: za22h11.r1 Soares fetal liver spleen 3.05 433972 AI878910 Hs.3688 cisplatin resistance-associated overexpr 3.04 427704 AW971063 Hs.292882 ESTs 3.03 440255 AI932285 Hs.160569 ESTs 3.03 424542 AI860558 Hs.272009 ESTs, Weakly similar to ALU2_HUMAN ALU S 3.03 413822 R08950 Hs.272044 ESTs, Weakly similar to ALU1_HUMAN ALU S 3.02 433944 AL117518 Hs.3686 KIAA0978 protein 3.01 440428 BE560954 gb: 601347719F1 NIH_MGC_8 Homo sapiens cD 3.00 #“average” normal colon tissues was greater than or equal to 3.0. The “average” colon cancer derived liver metastases level was set to the 50th percentile. The “average” normal colon tissue level was set to the 50th percentile.

[0350] TABLE 21A Pkey CAT Number Accession 409760 115373_1 AA302840 T93016 T92950 AA077551 413497 1373771_1 BE177661 H06215 BE144709 BE144829 417670 1692163_1 R07785 T85948 T86972 418876 179960_1 AA740616 AA654854 AA229923 419145 182217_1 N99638 AW973750 AA328271 H90994 AA558020 AA234435 N59599 R94815 423974 233842_1 AL118754 AA333202 H38001 430068 312849_1 AA464964 M85405 AA947566 432340 345248_1 AA534222 AA632632 T81234 433586 370470_1 T85301 AW517087 AA601054 BE073959 434280 382816_1 BE005398 AA628622 AA994155 434966 396504_1 AA657494 AI582663 AI581639 438962 467390_1 BE046594 BE046667 AA828585 AI207343 439848 477806_1 AW979249 D63277 AA846968 440428 49370_−1 BE560954 440638 499025_1 AI376551 T87714 AA897445 456332 179104_1 AA228357 AW841786 AW841716 # and Alignment Tools (DoubleTwist, Oakland California). The Genbank accession numbers for sequences comprising each cluster are listed in the “Accession” column.

[0351] TABLE 21B Pkey Ref Strand Nt_position 404571 7249169 Minus 112450-112648

[0352] TABLE 22 177 GENES DOWN-REGULATED IN COLON CANCER DERIVED LIVER METASTASES COMPARED TO NORMAL COLON TISSUE Pkey ExAccn UnigeneID Unigene Title R1 425196 AL037915 Hs.155097 carbonic anhydrase II 0.03 414522 AW518944 Hs.76325 step II splicing factor SLU7 0.03 409153 W03754 Hs.50813 hypothetical protein FLJ20022 0.03 452594 AU076405 Hs.29981 solute carrier family 26 (sulfate transp 0.03 424326 NM_014479 Hs.145296 disintegrin protease 0.04 414798 AI286323 Hs.97411 hypothetical protein MGC12335 0.04 432150 AK000224 Hs.272789 hypothetical protein FLJ20217 0.04 425206 NM_002153 Hs.155109 hydroxysteroid (17-beta) dehydrogenase 2 0.05 437145 AF007216 Hs.5462 solute carrier family 4, sodium bicarbon 0.05 447513 AW955776 Hs.313500 ESTs, Moderately similar to ALU7_HUMAN A 0.05 414807 AI738616 Hs.77348 hydroxyprostaglandin dehydrogenase 15-(N 0.06 428934 AF039401 Hs.194659 chloride channel, calcium activated, fam 0.06 432251 AW972983 Hs.232165 polycythemia rubra vera 1; cell surface 0.07 431727 AW293464 Hs.162031 ESTs 0.07 421515 Y11339 Hs.105352 GalNAc alpha-2, 6-sialyltransferase I, I 0.07 414555 N98569 Hs.76422 phospholipase A2, group IIA (platelets, 0.08 412047 AA934589 Hs.49696 ESTs 0.08 412056 T28160 Hs.778 guanylate cyclase activator 1B (retina) 0.08 422440 NM_004812 Hs.116724 aldo-keto reductase family 1, member B10 0.08 450684 AA872605 Hs.25333 interleukin 1 receptor, type II 0.09 418935 T28499 Hs.89485 carbonic anhydrase IV 0.09 433658 L03678 Hs.156110 immunoglobulin kappa constant 0.09 422260 AA315993 Hs.105484 regenerating gene type IV 0.09 433336 AF017986 Hs.31386 secreted frizzled-related protein 2 0.09 426784 U03749 Hs.172216 chromogranin A (parathyroid secretory pr 0.09 441888 AI733306 Hs.128071 hypothetical protein FLJ21302 0.10 440624 AF017987 Hs.7306 secreted frizzled-related protein 1 0.10 420929 AI694143 Hs.296251 programmed cell death 4 0.10 429970 AK000072 Hs.227059 chloride channel, calcium activated, fam 0.10 417233 W25005 Hs.24395 small inducible cytokine subfamily B (Cy 0.10 414802 AI793107 Hs.27018 Ris 0.10 424566 M16801 Hs.1790 nuclear receptor subfamily 3, group C, m 0.11 421996 AW583807 Hs.1460 glucagon 0.11 423371 AU076819 Hs.1650 solute carrier family 26, member 3 0.11 406741 AA058357 Hs.74466 carcinoembryonic antigen-related cell ad 0.11 414176 BE140638 Hs.75794 endothelial differentiation, lysophospha 0.11 408741 M73720 Hs.646 carboxypeptidase A3 (mast cell) 0.11 424527 AW138558 Hs.267158 ESTs, Weakly similar to I54374 gene NF2 0.12 426682 AV660038 Hs.2056 UDP glycosyltransferase 1 family, polype 0.12 453967 AW009077 Hs.232947 ESTs 0.12 425920 AL049977 Hs.162209 claudin 8 0.13 408134 AK000184 Hs.42945 acid sphingomyelinase-like phosphodieste 0.13 457407 AA505035 Hs.195651 ESTs 0.13 446500 U78093 Hs.15154 sushi-repeat-containing protein, X chrom 0.14 422487 AJ010901 Hs.198267 mucin 4, tracheobronchial 0.14 409196 NM_001874 Hs.334873 carboxypeptidase M 0.14 416426 AA180256 Hs.210473 Homo sapiens cDNA FLJ14872 fis, clone PL 0.14 406636 L12064 gb: Homo sapiens (clone WR4.12VL) anti-th 0.14 457982 AW856093 Hs.183617 ESTs 0.14 407744 AB020629 Hs.38095 ATP-binding cassette, sub-family A (ABC1 0.14 430378 Z29572 Hs.2556 tumor necrosis factor receptor superfami 0.14 424885 AI333771 Hs.82204 ESTs 0.14 423555 AW958201 Hs.178589 hepatocellular carcinoma antigen gene 52 0.14 444237 AA336878 Hs.9842 Human DNA sequence from clone RP4-788L20 0.14 445848 AA774824 Hs.13377 Homo sapiens clone 23649 and 23755 unkno 0.14 451062 AL110125 Hs.25910 Homo sapiens mRNA; cDNA DKFZp564C1416 (f 0.14 436485 X59135 Hs.156110 immunoglobulin kappa constant 0.14 423655 AA722425 Hs.182785 ESTs, Moderately similar to 1207289A rev 0.15 417332 AW972717 Hs.288462 hypothetical protein FLJ21511 0.15 427506 AK000134 Hs.179100 hypothetical protein FLJ20127 0.15 430712 AW044647 Hs.196284 ESTs 0.15 421666 AL035250 Hs.1408 endothelin 3 0.16 425692 D90041 Hs.155956 N-acetyltransferase 1 (arylamine N-acety 0.16 429412 NM_006235 Hs.2407 POU domain, class 2, associating factor 0.16 433745 AF075320 Hs.28980 hypothetical protein FLJ14540 0.16 450085 AW293791 Hs.60162 Homo sapiens cDNA: FLJ21528 fis, clone C 0.16 417820 D87449 Hs.82635 UDP-glucuronic acid/UDP-N-acetylgalactos 0.16 406722 H27498 Hs.293441 Homo sapiens SNC73 protein (SNC73) mRNA, 0.16 426488 X03350 Hs.4 alcohol dehydrogenase 1B (class I), beta 0.16 436327 AA813075 Hs.120181 ESTs 0.16 408873 AL0A6017 Hs.182278 calmodulin 2 (phosphorylase kinase, delt 0.16 429524 AB033037 Hs.205293 KIAA1211 protein 0.16 447023 AA356764 Hs.17109 integral membrane protein 2A 0.17 424264 D80400 Hs.239388 Human DNA sequence from clone RP1-304B14 0.17 410310 J02931 Hs.62192 coagulation factor III (thromboplastin, 0.17 432563 NM_013261 Hs.198468 peroxisome proliferative activated recep 0.17 406897 M57417 gb: Homo sapiens mucin (mucin) mRNA, part 0.17 451096 BE383234 Hs.25925 Homo sapiens, clone MGC: 15393, mRNA, com 0.17 447726 AL137638 Hs.19366 matrilin 2 0.17 409549 AB029015 Hs.54886 phospholipase C, epsilon 2 0.17 433334 AI927208 Hs.231958 matrix metalloproteinase 28 0.17 425849 AJ000512 Hs.296323 serum/glucocorticoid regulated kinase 0.17 407360 X13075 gb: Human 2a12 mRNA for kappa-immunoglobu 0.17 430627 U61148 Hs.247685 atonal homolog 1 (Drosophila) 0.17 418807 NM_004944 Hs.88646 deoxyribonuclease I-like 3 0.18 453399 Z70295 Hs.32966 guanylate cyclase activator 2B (uroguany 0.18 422994 AW891802 Hs.296276 ESTs 0.18 432134 AI816782 Hs.122583 hypothetical protein FLJ21934 0.18 400417 X72475 0.18 443506 H10661 Hs.192124 ESTs, Weakly similar to I38022 hypotheti 0.18 428470 AC002301 Hs.184507 Homo sapiens Chromosome 16 BAC clone CIT 0.18 451928 AI823801 Hs.30315 CTCL tumor antigen se57-1 0.18 429576 BE242628 Hs.209061 sudD (suppressor of bimD6, Aspergillus n 0.18 422106 D84239 Hs.111732 Fc fragment of IgG binding protein 0.19 430304 AL122071 Hs.238927 Homo sapiens mRNA; CDNA DKFZp434H1235 (f 0.19 452852 AK001972 Hs.30822 hypothetical protein FLJ11110 0.19 421904 BE143533 Hs.109309 hypothetical protein FLJ20035 0.19 417165 R80137 Hs.302738 Homo sapiens cDNA: FLJ21425 fis, clone C 0.19 417771 AA804698 Hs.82547 retinoic acid receptor responder (tazaro 0.19 452802 AU076403 Hs.323468 electron-transferring-flavoprotein dehyd 0.19 450680 AF131784 Hs.25318 Homo sapiens clone 25194 mRNA sequence 0.19 420061 AW024937 Hs.29410 ESTs 0.19 426828 NM_000020 Hs.172670 activin A receptor type II-like 1 0.19 408190 AB032963 Hs.43577 ATPase, Class I, type 8B, member 2 0.19 437682 AA476652 Hs.94952 Homo sapiens cDNA: FLJ23371 fis, clone H 0.19 449110 H56112 gb: yq95f07.r1 Soares fetal liver spleen 0.19 446727 AB011095 Hs.16032 KIAA0523 protein 0.19 408395 BE072425 Hs.44579 hypothetical protein FLJ20199 0.20 423541 AA296922 Hs.129778 gastrointestinal peptide 0.20 410850 AW362867 Hs.302738 Homo sapiens cDNA: FLJ21425 fis, clone C 0.20 412420 AL035668 Hs.73853 bone morphogenetic protein 2 0.20 423942 AF209704 Hs.135723 glycolipid transfer protein 0.20 421832 NM_016098 Hs.108725 HSPC040 protein 0.20 459046 AA910339 Hs.26216 LOC50627 0.20 421360 AA297012 Hs.103839 erythrocyte membrane protein band 4.1-li 0.20 438091 AW373062 Hs.83623 nuclear receptor subfamily 1, group I, m 0.20 403047 0.20 421712 AK000140 Hs.107139 hypothetical protein 0.20 427333 AF067797 Hs.176658 aquaporin 8 0.20 421964 X73079 Hs.288579 polymeric immunoglobulin receptor 0.20 438089 W05391 Hs.83623 nuclear receptor subfamily 1, group I, m 0.21 445200 AA084460 Hs.12409 somatostatin 0.21 404854 0.21 426390 AA377299 Hs.90431 ESTs 0.21 403381 0.21 449833 R82252 Hs.106106 protein kinase (cAMP-dependent, catalyti 0.21 457718 F18572 Hs.22978 ESTs, Weakly similar to ALU4_HUMAN ALU S 0.21 435730 AB020635 Hs.4984 KIAA0828 protein 0.21 431518 AA743462 Hs.165337 ESTs 0.21 412589 R28660 Hs.24305 ESTs 0.21 432584 AA928829 Hs.47099 hypothetical protein FLJ21212 0.21 426088 AF038007 Hs.166196 ATPase, Class I, type 8B, member 1 0.21 429143 AA333327 Hs.197335 plasma glutamate carboxypeptidase 0.21 414429 R51494 Hs.71818 ESTs 0.22 439670 AF088076 Hs.59507 ESTs, Weakly similar to AC004858 3 U1 sm 0.22 406697 M21388 Hs.123017 Human unproductively rearranged Ig mu-ch 0.22 406663 U24683 Hs.302063 immunoglobulin heavy constant mu 0.22 407811 AW190902 Hs.40098 cysteine knot superfamily 1, BMP antagon 0.22 417880 BE241595 Hs.82848 selectin L (lymphocyte adhesion molecule 0.22 430107 AA465293 Hs.105069 ESTs 0.22 424273 W40460 Hs.144442 phospholipase A2, group X 0.22 419559 Y07828 Hs.91096 ring finger protein 0.22 413517 N76712 Hs.44829 ESTs, Weakly similar to I38022 hypotheti 0.22 407243 AA058357 Hs.74466 carcinoembryonic antigen-related cell ad 0.22 433906 AI167816 Hs.43355 ESTs 0.22 446203 Z47553 Hs.14286 flavin containing monooxygenase 5 0.22 403740 0.22 405701 0.22 413554 AA319146 Hs.75426 secretogranin II (chromogranin C) 0.22 419577 L36531 Hs.91296 integrin, alpha 8 0.23 451820 AW058357 Hs.337353 ESTs 0.23 424897 D63216 Hs.153684 frizzled-related protein 0.23 422880 AF228704 Hs.121524 glutathione reductase 0.23 430832 AI073913 Hs.100686 ESTs, Weakly similar to JE0350 Anterior 0.23 430753 AI432401 Hs.2659 fibrinogen-like 2 0.23 409060 AI815867 Hs.50130 necdin (mouse) homolog 0.23 412228 AW503785 Hs.73792 complement component (3d/Epstein Barr vi 0.24 414171 AA360328 Hs.865 RAP1A, member of RAS oncogene family 0.24 417916 NM_006416 Hs.82921 solute carrier family 35 (CMP.sialic aci 0.24 414589 AA149791 Hs.68864 ESTs, Weakly similar to phosphatidylseri 0.24 427167 AI239607 Hs.99196 hypothetical protein MGC11324 0.24 440630 BE561430 Hs.239388 Human DNA sequence from clone RP1-304B14 0.24 423044 AA320829 Hs.97266 protocadherin 18 0.24 441931 BE564830 Hs.23744 hypothetical protein FLJ12899 0.24 443060 D78874 Hs.8944 procollagen C-endopeptidase enhancer 2 0.24 405441 0.24 407241 M34516 gb: Human omega light chain protein 14.1 0.24 415165 AW887604 Hs.78065 complement component 7 0.24 426447 AV655843 Hs.169919 electron-transfer-flavoprotein, alpha po 0.24 410748 BE383816 Hs.12532 chromosome 1 open reading frame 21 0.24 436032 AA150797 Hs.109276 latexin protein 0.24 414256 AW410035 Hs.75862 MAD (mothers against decapentaplegic, Dr 0.24 414197 W44877 Hs.55501 ESTs 0.24 406836 AW514501 Hs.156110 immunoglobulin kappa constant 0.24 437083 AW082597 Hs.244862 ESTs 0.25 421709 AA159394 Hs.107056 CED-6 protein 0.25 426512 AW511656 Hs.170177 Meis1 (mouse) homolog 0.25 #liver metastases to “average” normal colon tissues was less than or equal to 0.25. The “average” colon cancer derived liver metastases level was set to the 50th percentile. The “average” normal adult tissue level was set to the 50th percentile.

[0353] TABLE 22A Table 22A shows the accession numbers for those pkeys lacking unigeneID's for Tables 21A. For each probeset we have listed the gene cluster number from which the oligonucleotides were designed. Gene clusters were compiled using sequences derived from Genbank ESTs and mRNAs. These sequences were clustered based on sequence similarity using Clustering and Alignment Tools (DoubleTwist, Oakland California). The Genbank accession numbers for sequences comprising each cluster are listed in the “Accession” column. Pkey: Unique Eos probeset identifier number CAT number: Gene cluster number Accession: Genbank accession numbers Pkey CAT Number Accession 449110 798430_1 H56112 H58047 AI630710 N58742

[0354] TABLE 22B Pkey: Unique number corresponding to an Eos probeset Ref: Sequence source. The 7 digit numbers in this column are Genbank Identifier (GI) numbers. “Dunham I. et al.” refers to the publication entitled “The DNA sequence of human chromosome 22.” Dunham I. et al., Nature (1999) 402:489-495. Strand: Indicates DNA strand from which exons were predicted. Nt_position: Indicates nucleotide positions of predicted exons. Pkey Ref Strand Nt_position 403047 3540153 Minus 59793-59968 403381 9438267 Minus 26009-26178 403740 7630882 Plus 86504-87227 404854 7143420 Plus 14260-14537 405441 7408124 Plus 100952-101283 405701 4263751 Plus 93243-93354

[0355] TABLE 23 175 GENES UP-REGULATED IN COLON CANCER DERIVED LIVER METASTASES COMPARED TO COLON CANCER PRIMARY TUMOR SAMPLES CLASSIFIED AS DUKE'S B SURVIVOR Table 23 shows 175 genes up-regulated in colon cancer derived liver metastases compared to colon cancer primary tumor samples classified as Duke's B stage with a positive survival outcome (Duke's B survivor). These were selected from 59680 probesets on the Affymetrix/Eos Hu03 GeneChip array such that the ratio of “average” colon cancer derived liver metastases to “average” Duke's B survivor was greater than or equal to 3.0. The “average” colon cancer derived liver metastases level was set to the 50th percentile. The “average” Duke's B survivor level was set to the 50th percentile. Pkey: Unique Eos probeset identifier number ExAccn: Exemplar Accession number, Genbank accession number UnigeneID: Unigene number Unigene Title: Unigene gene title R1: Genes up liver metastases vs Duke's B survivors Pkey ExAccn UnigeneID Unigene Title R1 426101 AL049987 Hs.166361 Homo sapiens mRNA; cDNA DKFZp564F112 (fr 9.06 432572 AI660840 Hs.191202 ESTs, Weakly similar to ALUE_HUMAN !!!! 7.96 424878 H57111 Hs.221132 ESTs 7.88 428046 AW812795 Hs.155381 ESTs, Moderately similar to I38022 hypot 7.48 407284 AI539227 Hs.214039 hypothetical protein FLJ23556 7.45 439943 AW083789 Hs.124620 ESTs 7.00 442369 AI565071 Hs.159983 ESTs 7.00 415116 AA160383 Hs.269956 ESTs 6.98 433517 AW022133 Hs.189838 ESTs 6.70 437176 AW176909 Hs.42346 calcineurin-binding protein calsarcin-1 6.68 440524 R71264 Hs.16798 ESTs 6.62 408806 AW847814 Hs.289005 Homo sapiens cDNA: FLJ21532 fis, clone C 6.38 448974 AL049390 Hs.22689 Homo sapiens mRNA; cDNA DKFZp586O1318 (f 6.28 412088 AI689496 Hs.108932 ESTs 6.04 417670 R07785 gb:yf15c06.r1 Soares fetal liver spleen 5.95 440774 AI420611 Hs.127832 ESTs 5.91 426086 T94907 Hs.188572 ESTs 5.90 436100 AA704806 Hs.143842 ESTs, Weakly similar to 2004399A chromos 5.84 453204 R10799 Hs.191990 ESTs 5.84 407289 AA135159 Hs.203349 Homo sapiens cDNA FLJ12149 fis, clone MA 5.67 432435 BE218886 Hs.282070 ESTs 5.61 434963 AW974957 Hs.288719 Homo sapiens cDNA FLJ12142 fis, clone MA 5.60 421221 AW276914 Hs.326714 Homo sapiens clone IMAGE:713177, mRNA se 5.54 407328 AA508857 Hs.187748 ESTs, Weakly similar to ALU1_HUMAN ALU S 5.51 440980 AL042005 Hs.1117 tripeptidyl peptidase II 5.48 443651 W22152 Hs.282929 ESTs 5.42 412668 AA456195 Hs.10056 hypothetical protein FLJ14621 5.29 444838 AV651680 Hs.208558 ESTs 5.24 433312 AI241331 Hs.131765 ESTs, Moderately similar to I38937 DNA/R 5.11 430665 BE350122 Hs.157367 ESTs, Weakly similarto I78885 serine/th 5.11 434966 AA657494 gb:nt66f04.s1 NCI_CGAP_Pr3 Homo sapiens 5.10 426897 AW976570 Hs.97387 ESTs 5.08 432954 AI076345 Hs.214199 ESTs 5.07 431416 AA532718 Hs.178604 ESTs 5.00 420717 AA284447 Hs.271887 ESTs 4.96 424950 AA602917 Hs.156974 ESTs 4.94 438962 BE046594 gb:hn41c11.x1 NCI_CGAP_RDF2 Homo sapiens 4.92 419999 AI760942 Hs.191754 ESTs 4.89 435812 AA700439 Hs.188490 ESTs 4.86 418662 AI801098 Hs.151500 ESTs 4.79 428065 AI634046 Hs.157313 ESTs 4.77 407618 AW054922 Hs.53478 Homo sapiens cDNA FLJ12366 fis, clone MA 4.75 435981 H74319 Hs.188620 ESTs 4.74 419145 N99638 gb:za39g11.r1 Soares fetal liver spleen 4.73 432340 AA534222 gb:nj21d02.s1 NCI_CGAP_AA1 Homo sapiens 4.72 447982 H22953 Hs.137551 ESTs 4.72 449509 AA001615 Hs.84561 ESTs 4.72 407946 AA226495 Hs.154292 ESTs 4.70 438607 AW080237 Hs.252884 ESTs 4.68 438406 BE273296 Hs.254467 Homo sapiens cDNA FLJ13255 fis, clone OV 4.62 426818 AA554827 Hs.289115 DKFZp434A0131 protein 4.62 452220 BE158006 Hs.212296 ESTs 4.60 436823 AW749865 Hs.293645 ESTs, Weakly similar to I38022 hypotheti 4.60 433854 AA610649 Hs.333239 ESTs 4.56 413816 AW958181 Hs.189998 ESTs 4.52 428079 AA421020 Hs.208919 ESTs 4.52 421097 AI280112 Hs.125232 Homo sapiens cDNA FLJ13266 fis, clone OV 4.50 417035 AA192455 Hs.22968 pi Homo sapiens clone IMAGE:451939, mRNA se 4.48 423974 AL118754 gb:DKFZp761P1910_r1 761 (synonym: hamy2) 4.44 449618 AI076459 Hs.15978 KIAA1272 protein 4.44 431615 AW295859 Hs.235860 ESTs 4.44 418876 AA740616 gb:ny97f11.s1 NCI_CGAP_GCB1 Homo sapiens 4.43 428279 AA425310 Hs.155766 ESTs, Weakly similar to A47582 B-cell gr 4.42 430573 AA744550 Hs.136345 ESTs 4.42 430929 AA489166 Hs.156933 ESTs 4.40 446099 T93096 Hs.17126 hypothetical protein MGC15912 4.40 439362 AI954880 Hs.134604 ESTs 4.36 421999 U50535 Hs.110630 Human BRCA2 region, mRNA sequence CG006 4.35 434220 AI174777 Hs.283039 Homo sapiens PRO2492 mRNA, complete cds 4.33 432925 AA878324 Hs.192734 ESTs 4.32 417819 AI253112 Hs.133540 ESTs 4.30 426848 H72531 Hs.36190 ESTs 4.30 429831 AA564489 Hs.137526 ESTs 4.30 433735 AA608955 Hs.109653 ESTs 4.30 418884 AA230228 Hs.59197 ESTs 4.28 413243 AA769266 Hs.193657 ESTs 4.26 431749 AL049263 Hs.306292 Homo sapiens mRNA; cDNA DKFZp564F133 (fr 4.23 428054 AI948688 Hs.266619 ESTs 4.22 413967 AW204431 Hs.117853 ESTs, Weakly similar to I38022 hypotheti 4.22 433230 AW136134 Hs.220277 ESTs 4.22 421057 T58283 Hs.10450 Homo sapiens cDNA: FLJ22063 fis, clone H 4.22 423578 AW960454 Hs.222830 ESTs 4.21 439717 W94472 Hs.59529 ESTs, Moderately similar to ALU1_HUMAN A 4.20 443696 AW607444 Hs.134622 ESTs 4.20 432722 AA830532 Hs.326160 ESTs 4.18 435756 AI418466 Hs.33665 ESTs 4.14 428825 AI084336 Hs.128783 ESTs, Weakly similar to I38022 hypotheti 4.14 439451 AF086270 Hs.278554 heterochromatin-like protein 1 4.12 445943 AW898533 Hs.181574 ESTs 4.12 450219 AI826999 Hs.224624 ESTs 4.12 431379 AA504264 Hs.182937 peptidylprolyl isomerase A (cyclophilin 4.11 432451 AW972771 Hs.292471 ESTs, Weakly similar to ALU1_HUMAN ALU S 4.10 443148 AI034357 Hs.211194 ESTs, Weakly similar to ALU8_HUMAN ALU S 4.08 450177 AI698091 Hs.107845 ESTs 4.08 420911 U77413 Hs.100293 O-linked N-acetylglucosamine (GlcNAc) tr 4.06 421114 AW975051 Hs.293156 ESTs, Weakly similar to I78885 serine/th 4.06 432731 R31178 Hs.287820 fibronectin 1 4.06 433588 AI056872 Hs.133386 ESTs 4.06 434658 AI624436 Hs.310286 ESTs 4.06 444040 AF204231 Hs.182982 golgin-67 4.06 429512 AA453987 Hs.144802 ESTs 4.06 443349 AI052572 Hs.269864 ESTs, Weakly similar to ALU1_HUMAN ALU S 4.04 439867 AA847510 Hs.161292 ESTs 4.04 425955 T96509 Hs.248549 ESTs, Moderately similar to S65657 alpha 4.02 431393 AW971493 Hs.134269 ESTs, Highly similar to cytokine recepto 4.00 432125 AW972667 Hs.287510 Homo sapiens cDNA FLJ12300 fis, clone MA 4.00 435468 AW362803 Hs.166271 ESTs 3.97 412059 AA317962 Hs.249721 ESTs, Moderately similar to PC4259 ferri 3.95 446682 AW205632 Hs.211198 ESTs 3.95 441328 AI982794 Hs.159473 ESTs 3.92 455778 BE088746 gb:CM2-BT0693-210300-123-d09 BT0693 Homo 3.90 438996 AW748336 Hs.168052 KIAA0421 protein 3.86 418303 AA215701 Hs.186541 ESTs, Weakly similar to I38022 hypotheti 3.85 444816 Z48633 Hs.283742 H.sapiens mRNA for retrotransposon 3.84 429355 AW973253 Hs.292689 ESTs 3.83 438578 AA811244 Hs.164168 ESTs 3.83 432945 AL043683 Hs.8173 hypothetical protein FLJ10803 3.83 435318 T97301 Hs.18026 ESTs 3.82 449941 AW450536 Hs.209260 ESTs 3.80 424915 R42755 Hs.23096 ESTs 3.76 449987 AW079749 Hs.184719 ESTs, Weakly similar to ALU1_HUMAN ALU S 3.76 416265 AA177088 Hs.190065 ESTs 3.75 413497 BE177661 gb:RC1-HT0598-020300-011-h02 HT0598 Homo 3.74 412093 BE242691 Hs.14947 ESTs 3.74 413822 R08950 Hs.272044 ESTs, Weakly similar to ALU1_HUMAN ALU S 3.73 431915 AK000777 Hs.272197 Homo sapiens cDNA FLJ20770 fis, clone CO 3.68 434442 AA737415 Hs.152826 ESTs 3.63 434959 AW974949 Hs.186564 ESTs, Weakly similar to I38022 hypotheti 3.63 427704 AW971063 Hs.292882 ESTs 3.62 426510 AW861225 Hs.194637 BANP homolog, SMAR1 homolog 3.60 435714 AA699325 Hs.269880 ESTs 3.60 432598 AI341227 Hs.157106 ESTs 3.57 438543 AA810141 Hs.192182 ESTs 3.55 422068 AI807519 Hs.104520 Homo sapiens cDNA FLJ13694 fis, clone PL 3.54 418259 AA215404 Hs.137289 ESTs 3.54 428290 AI932995 Hs.183475 Homo sapiens clone 25061 mRNA sequence 3.49 419457 AA243146 Hs.209334 ESTs, Moderately similar to S23A_HUMAN P 3.47 439312 AA833902 Hs.270745 ESTs 3.47 408784 AW971350 Hs.63388 ESTs 3.45 456332 AA228357 gb:nc39d05.r1 NCI_CGAP_Pr2 Homo sapiens 3.45 424762 AL119442 Hs.183684 eukaryotic translation initiation factor 3.44 442884 AI076570 Hs.134053 ESTs 3.44 421023 AW449855 Hs.96557 Homo sapiens cDNA FLJ12727 fis, clone NT 3.43 434575 AI133446 Hs.299964 Homo sapiens clone FLB7723 PRO2055 mRNA, 3.42 430433 AA478883 Hs.273766 ESTs 3.39 419317 AA236282 Hs.172318 ESTs 3.38 448710 T62926 Hs.304184 ESTs 3.37 439322 H72245 Hs.188635 ESTs 3.37 430332 R51790 Hs.239483 Human clone 23933 mRNA sequence 3.35 411755 BE327036 Hs.117494 ESTs 3.33 427882 AA640987 Hs.193767 ESTs 3.28 438899 AF085833 Hs.135624 ESTs 3.28 436535 AW295687 Hs.254420 ESTs 3.25 434936 AI285970 Hs.183817 ESTs 3.22 451730 AF095887 Hs.26937 brain and nasopharyngeal carcinoma susce 3.18 447514 AI809314 Hs.208501 ESTs, Weakly similar to B34087 hypotheti 3.18 413672 BE156536 gb:QV0-HT0368-310100-091-h10 HT0368 Homo 3.16 435073 AA664078 gb:ac04a05.s1 Stratagene lung (937210) H 3.13 450295 AI766732 Hs.210628 ESTs 3.13 419341 N71463 Hs.118888 ESTs, Weakly similar to ALU1_HUMAN ALU S 3.13 434495 AW352170 Hs.129086 Homo sapiens cDNA FLJ12007 fis, clone HE 3.12 408113 T82427 Hs.194101 Homo sapiens cDNA: FLJ20869 fis, clone A 3.12 456437 AI924228 Hs.115185 ESTs, Moderately similarto PC4259 ferri 3.12 421489 AI922821 Hs.32433 ESTs 3.12 436090 AI640635 Hs.116468 EST 3.11 450230 AW016607 Hs.201582 ESTs 3.11 436011 BE466173 Hs.145696 splicing factor (CC1.3) 3.09 418720 AI381687 Hs.39526 ESTs 3.09 433102 AI343966 Hs.158528 ESTs 3.08 436150 AW510927 Hs.125243 ESTs 3.05 440116 AI798851 Hs.283108 hemoglobin, gamma G 3.04 414900 AW452420 Hs.245678 ESTs 3.04 435937 AA830893 Hs.119769 ESTs 3.02 424848 AI263231 Hs.327090 EST 3.02 435354 AA678267 Hs.117115 ESTs 3.00

[0356] TABLE 23A Table 23A show the accession numbers for those pkeys lacking unigeneID's for tables 1-20A, 21A, 22A, and 23A. For each probeset we have listed the gene cluster number from which the oligonucleotides were designed. Gene clusters were compiled using sequences derived from Genbank ESTs and mRNAs. These sequences were clustered based on sequence similarity using Clustering and Alignment Tools (DoubleTwist, Oakland California). The Genbank accession numbers for sequences comprising each cluster are listed in the “Accession” column. Pkey: Unique Eos probeset identifier number CAT number: Gene cluster number Accession: Genbank accession numbers Pkey CAT Number Accession 413497 1373771_1 BE177661 H06215 BE144709 BE144829 413672 1382512_1 BE156536 BE156439 BE156700 BE156449 BE156653 BE156533 BE156524 BE156670 BE156721 BE156723 417670 1692163_1 R07785 T85948 T86972 418876 179960_1 AA740616 AA654854 AA229923 419145 182217_1 N99638 AW973750 AA328271 H90994 AA558020 AA234435 N59599 R94815 423974 233842_1 AL118754 AA333202 H38001 432340 345248_1 AA534222 AA632632 T81234 434966 396504_1 AA657494 AI582663 AI581639 435073 399701_1 AA664078 AW363313 AA805009 438962 467390_1 BE046594 BE046667 AA828585 AI207343 455778 1364506_1 BE088746 BE088802 BE088755 BE088876 BE088947 BE088881 BE088952 456332 179104_1 AA228357 AW841786 AW841716

[0357] TABLE 24 34 GENES DOWN-REGULATED IN COLON CANCER DERIVED LIVER METASTASES COMPARED TO COLON CANCER PRIMARY TUMOR SAMPLES CLASSIFIED AS DUKE'S B SURVIVOR Table 24 shows 34 genes down-regulated in colon cancer derived liver metastases compared to colon cancer primary tumor samples classified as Duke's B stage with a positive survival outcome (Duke's B survivor). These were selected from 59680 probesets on the Affymetrix/Eos Hu03 GeneChip array such that the ratio of “average” colon cancer derived liver metastases to “average” Duke's B survivor was greater than or equal to 0.25. The “average” colon cancer derived liver metastases level was set to the 50th percentile. The “average” Duke's B survivor level was set to the 50th percentile. Pkey: Unique Eos probeset identifier number ExAccn: Exemplar Accession number, Genbank accession number UnigeneID: Unigene number Unigene Title: Unigene gene title R1: Genes down liver metastases vs Duke's B survivors Pkey ExAccn UnigeneID Unigene Title R1 414522 AW518944 Hs.76325 step II splicing factor SLU7 0.05 416768 AA363733 Hs.1032 regenerating islet-derived 1 alpha (panc 0.07 409153 W03754 Hs.50813 hypothetical protein FLJ20022 0.07 414555 N98569 Hs.76422 phospholipase A2, group IIA (platelets, 0.11 418007 M13509 Hs.83169 matrix metalloproteinase 1 (interstitial 0.11 424326 NM_014479 Hs.145296 disintegrin protease 0.11 428934 AF039401 Hs.194659 chloride channel, calcium activated, fam 0.12 417233 W25005 Hs.24395 small inducible cytokine subfamily B (Cy 0.12 422260 AA315993 Hs.105484 regenerating gene type IV 0.12 425196 AL037915 Hs.155097 carbonic anhydrase II 0.13 433336 AF017986 Hs.31386 secreted frizzled-related protein 2 0.13 450685 L15533 Hs.423 pancreatitis-associated protein 0.14 407811 AW190902 Hs.40098 cysteine knot superfamily 1, BMP antagon 0.15 414798 AI286323 Hs.97411 hypothetical protein MGC12335 0.16 452852 AK001972 Hs.30822 hypothetical protein FLJ11110 0.17 447513 AW955776 Hs.313500 ESTs, Moderately similar to ALU_HUMAN A 0.17 423541 AA296922 Hs.129778 gastrointestinal peptide 0.17 425071 NM_013989 Hs.154424 deiodinase, iodothyronine, type II 0.18 406636 L12064 gb:Homo sapiens (clone WR4.12VL) anti-th 0.18 421515 Y11339 Hs.105352 GalNAc alpha-2, 6-sialyltransferase 1,1 0.18 428368 BE440042 Hs.83326 matrix metalloproteinase 3 (stromelysin 0.19 414812 X72755 Hs.77367 monokine induced by gamma interferon 0.20 452594 AU076405 Hs.29961 solute carrier family 26 (sulfate transp 0.20 428227 AA321649 Hs.2248 small inducible cytokine subfamily B (cy 0.21 408741 M73720 Hs.646 carboxypeptidase A3 (mast cell) 0.21 453064 R40334 Hs.89463 potassium large conductance calcium-acti 0.21 431727 AW293464 Hs.162031 ESTs 0.22 433658 L03678 Hs.156110 immunoglobulin kappa constant 0.22 442064 AI422867 Hs.88594 ESTs 0.22 417880 BE241595 Hs.52848 selectin L (lymphocyte adhesion molecule 0.22 430280 AA361258 Hs.237868 interteukin 7 receptor 0.23 452877 AI250789 Hs.32478 ESTs 0.23 410310 J02931 Hs.62192 coagulation factor III (thromboplastin, 0.24 402408 0.24

[0358] TABLE 24B Pkey: Unique number corresponding to an Eos probeset Ref: Sequence source. The 7 digit numbers in this column are Genbank Identifier (GI) numbers. “Dunham I. et al.” refers to the publication entitied “The DNA sequence of human chromosome 22.” Dunham I. et al., Nature (1999) 402:489-495. Strand: Indicates DNA strand from which exons were predicted. Nt_position: Indicates nucleotide positions of predicted exons. Pkey Ref Strand Nt_position 402408 9796239 Minus 110326-110491

[0359] TABLE 25 Table 25 depicts Seq ID No., UnigeneID, UnigeneTitle, Pkey, and ExAccn for all of the sequences in Table 26. Seq ID No links the nucleic acid and protein sequence information in Table 26 to Table 25. Pkey: Unique Eos probeset identifier number ExAccn: Exemplar Accession number, Genbank accession number UnigeneID: Unigene number Unigene Title: Unigene gene titie Seq.ID.No.: Sequence Identification Number found in Table 26 Pkey ExAccn UnigeneID Unigene Title Seq ID No. 426101 AL049987 Homo sapiens mRNA; cDNA DKFZp564F112 (fr 1-4 419145 N99638 gb 5 & 6 426818 AA554827 Hs.340046 DKFZp434A0131 protein 7 & 8 421057 T58283 Homo sapiens cDNA 9 446619 AU076643 Hs.313 secreted phosphoprotein 1 (osteopontin, 10 & 11 431958 X63629 Hs.2877 cadherin 3, type 1, P-cadherin (placenta 12 & 13 409041 AB033025 Hs.50081 Hypothetical protein, XP_051860 (KIAA119 14 & 15 443162 T49951 Hs.9029 DKFZP434G032 protein 16 & 17 436385 BE551618 Hs.144097 ESTs 18-20 447033 AI357412 Hs.157601 ESTs 21 & 22 439608 AW864696 Hs.301732 hypothetical protein MGC5306 23-27 449032 AA045573 Hs.22900 nuclear factor (erythroid-derived 2)-lik 28 & 29 442577 AA292998 Hs.163900 ESTs 30 & 31 429970 AK000072 Hs.227059 chloride channel, calcium activated, fam 32 & 33 424566 M16801 Hs.1790 nuclear receptor subfamily 3, group C, m 34 & 35 457407 AA505035 Hs.345911 ESTs 36 430378 Z29572 Hs.2556 tumor necrosis factor receptor superfami 37 & 38 417332 AW972717 Hs.288462 hypothetical protein FLJ21511 39 & 40

[0360] TABLE 25A Pkey: Unique Eos probeset identifier number CAT number Gene cluster number Accession: Genbank accession numbers Pkey CAT Number Accession 409041 10962_2 AB033025 AL359061 AL045836 AI751521 AI752804 AI752650 AA853580 AI752290 AA853460 AI752769 AA852309 AA853785 AA853219 AW068503 AI752069 AL049389 AW068368 6E439518 W52813 BE141833 AI940574 AI750606 AL109718 AA242845 AA315795 AA307741 AW954603 AI752070 AA350794 AI752649 AA307755 AW951677 AA298896 BE439692 AA852453 AW068826 AW853984 AA418236 AA639417 AW290917 AI750592 AI752768 AL045837 AI926513 AW262903 BE439819 AI459360 AW339074 AW295181 AW029483 AI750945 AI750659 AI752525 AI147688 BE440122 AI751522 AI473816 AI752291 AI694639 AI925816 AA599476 AA242752 AW021892 AI755098 AW469299 AW769363 AA853579 AI784082 AA852454 AI925501 AA976657 AW150473 AW166734 417332 166755_1 AW972717 AA523805 AI962905 AI373245 AW235545 AI812045 AW589434 AI826824 AW572339 AI377551 AA195718 AI868470 419145 182217_1 N99638 AW973750 AA328271 H90994 AA558020 AA234435 N59599 R94815 421057 198849_1 T58283 AA765038 AA283052 H99396 AA814751 AI032674 N81016 N81017 BE222349 AA830545 424566 2408_1 M16801 NM_000901 D57171 AL041328 AF068623 AI201179 AA151766 AA568349 AI698649 AI692765 BE327401 AA744953 AA744951 AW361986 AV651840 T29894 AW945145 AW945145 W24096 AI183952 AI458972 AW190993 AI765359 AI634663 AI741201 AW418944 AI767551 AA679687 AW772342 AW629508 BE504300 AI251790 AI522294 AA724341 AW615402 AI537570 AA470665 AI458375 AW768901 AA447079 T23537 AI783744 R44301 D56621 N91919 AA149749 426101 26088_1 AL049987 AW362842 T78981 AA247541 AI217018 AW961515 AA632986 AA663108 BE326465 AW872412 AI024889 AA453725 BE150458 AA229448 AA442638 AA442648 AI916737 AA480220 AA868553 AI827987 AI005467 R31132 AI742087 AA442379 N56349 AW769479 AI860142 AI917507 AA813604 AI860141 AI459289 AA522837 AI354470 AI921333 BE466760 AW971193 AW103830 AW277065 AW020895 AI187977 N28268 AI084517 R95914 AA833517 AA563934 AA437299 AA436880 AA447794 AA812876 AA663178 R31089 AI472712 R64648 AA600372 AA229164 AA703066 AW270324 AI191725 AA551512 AA493776 426818 272427_1 AA554827 AA701001 AW972954 AL039129 AA385540 AA911663 429970 31134_1 AK000072 AW840683 AW843764 AW844444 AW844515 AW603469 AW862395 AI860838 AW511708 AF127035 NM_012128 AK000138 430378 3170_1 Z29572 AW976377 AA286871 AA633372 AA987627 AA743176 AI865358 AJ006884 AF031845 Z14955 431958 3394_1 X63629 NM—001793 BE175433 BE153414 BE153425 AW364593 BE315317 AW950190 AA314252 BE142943 AW365220 AW368405 BE004269 AW366568 AL040609 AI829273 AI591168 BE146183 AI631060 AI830793 W78081 W92295 AI927422 BE009313 AI371793 AW993031 AI204659 AA535113 AW993030 AI190281 AA555159 AW269637 AW993146 AI149268 AA425217 AW473194 AI890930 AA551993 AI952106 W92308 AI827275 W45400 AI952328 AW609233 AA774611 AA551779 AI913967 AI798658 AI537658 AW517535 AA632236 AW339148 AW589522 AA836945 AA961263 AW015821 AW272946 C00249 W40333 BE143121 436385 418907_1 BE551618 AI207338 BE220568 AI261568 AW841737 AA714722 AA946891 AI033239 439608 47438_3 AW864696 AW338889 AI342866 AA084522 AI244150 AI610339 AA425635 AA764930 AA976965 AW805766 AA057765 AW805845 AW802595 AA262971 AI969620 N75323 BE549060 AW805725 AA025809 N80776 N64595 AW073372 AA025493 AI819475 AW028879 AW189496 AA442907 AW410368 AI911629 N71276 AW316922 AW805838 AA043880 AW189184 AA449758 AA748153 AA705608 AI910643 AA279492 BE160119 AW805761 AA026262 AA782207 AW057652 AW805768 H21998 AW194254 AW275178 AA449040 AA279582 N76314 N54348 442577 54549_1 AA292998 AW238350 AI676059 AW074092 BE566458 AW078677 AW514801 AW073701 AW170620 AI523736 AI580870 AI923975 AI393326 AI700229 AW450814 AW628452 AI671457 AA937534 AI889894 AW339423 AW291875 AA551874 AI682314 AI926227 AA397375 443162 5613_1 T49951 AA025326 H04839 AA393303 R63101 W57657 W25628 AI961431 R71165 N39940 H01548 H01759 AA641624 AI634930 AA595296 AW994770 AW994747 BE047247 W38159 AA858133 AI701944 AW386273 AA676625 R24676 R79410 AA922863 AI151319 H01013 AA024482 W02674 H01456 AI150858 AW135972 AW631167 AI270332 H04750 T49622 AA004543 R63061 AI093066 AI247539 H01225 H03388 AW472933 AA382448 AI219287 N27194 AW389613 AA649738 AW994764 AW389614 R25176 AA897262 R71626 AA909471 R71240 AW811917 R76109 AI202312 AI858010 R76162 AL117538 R79411 T58658 AW994674 446619 685_1 AU076643 AA594604 AA348866 R18197 AA345192 AA337773 AA089791 R84435 AA337838 AW392167 AA075190 D55416 AW150380 AW366257 AA579816 H93048 AW385889 AW385697 AI186216 AW581197 AL037509 AB019562 AA232626 R97905 AW368019 AA242891 AW888502 AI798331 AW385835 AW581221 T96947 H87989 AA369511 AA075191 R80742 AA366406 W92752 H45588 AI864016 AW888497 BE004992 AI384110 AI624258 AI627593 W92728 AI682719 AA948208 AA171734 N40517 J04765 AA379957 AA362403 NM_000582 AF052124 AA300290 AA333447 AA343721 AW889543 BE586767 R76601 R18015 AA100531 AA489963 AA101296 AA363513 AA344088 AA336750 T77505 D56440 AL110351 AL110331 F12195 R20175 AA336664 H17766 AA363538 AA363590 D28760 AW578517 AA383531 AI814667 AA846899 AA368253 AW951285 AA297992 AA327756 AW361609 AW815455 AW815427 AW815428 D54182 AW852200 AA171630 W27018 AW815864 AW379995 AW378222 AW362610 BE566022 AW021023 C17352 D58435 AA345409 AI623991 AW020967 AI924770 AI799443 AW946393 AA991239 AI571617 AI935181 AI923999 AI826895 AI860319 AW189873 AW270353 AW023584 AI813811 R99929 AW339056 AA913152 AI636352 AI829394 AW151077 AW192580 AI570119 AI086391 AW021764 AW519154 AI375193 AW268678 BE465690 AW019983 AW268654 AI573138 AI141809 AI954553 AI559242 AA568945 AA886417 AW338527 AI635881 BE465666 AI921239 AA968537 AI958027 AA911981 AI827661 AW511046 BE619780 AI922227 AI811870 AW190131 AW129220 AW512906 AI290757 AI819088 AI623771 AA775616 BE349419 AI126375 H88773 AI241758 AW275157 AI337848 AI613425 AI631387 AA922631 AI273483 AI982898 AW168957 AI446481 BE501588 BE048264 AI499922 AW023812 BE220523 AW973846 BE349276 AI141091 AA976060 AW973845 AA101270 AI582472 AW613675 AI139360 AI282627 AI276044 N22345 AI261875 AA634136 AI824468 AW887693 N27107 R21504 AI042223 N22067 AW196871 AI581019 BE004973 AA252035 N22087 AA570717 H11250 AI804026 AA368098 AA021512 H08842 N26275 AA176368 AI758758 AA570371 AA232574 BE221177 AW190221 AW471386 AA78225 AI422140 AI624521 AA719775 AA300291 AA568657 AI871430 BE465630 N71862 T72587 W92721 H88774 D64383 AW103693 AW089986 AI382689 R42363 R44962 T98770 AA357374 AW022074 AI356207 T29241 AW089431 AI933875 N66267 N67352 AA121786 AA363910 F09824 T95818 N66888 R80550 AI280887 AW196719 R59299 AW021049 H73469 AI954311 BE439454 AW079450 AW973850 AA348338 AW896006 AW268145 AA853631 H17650 R39537 N66873 N67240 H06298 AI784199 R44260 AA904118 AA911756 F04544 AA807809 AA665210 AI696448 T29719 AA837240 T64844 H08926 447033 704603_1 AI357412 AI870708 AI590539 W07459 449032 7945_1 AA045573 AA279920 R20139 AA372783 AW963629 H21473 R78318 W74359 AA022505 AA369091 AW084075 AA503638 AV660815 AI216262 AA779843 BE219825 AF125534 AW972129 AI919099 AI621283 AI300590 AI953701 AA331415 AW610546 AW793050 AI953679 AW793047 AW610543 AI671103 AW292105 AW024112 R77947 W76339 AA305111 AA132523 AA227467 H21401 AW366572 AW024129 AI701886 AI654744 BE042803 AI347173 AW866053 AW662710 R36639 AI469777 AA962733 AI865368 AA501998 AW866054 BE178974 457407 333252_1 AA505035 AW235098 AI634028

[0361] TABLE 26 Seq ID NO: 1 DNA sequence Nucleic Acid Accession #: see Table 25 & 25A for complete list 1    11    21    31    41    51 |   |   |   |   |   | CAATATAGTA CAATAACTAT TTGCATGACA TTTACATCGG ATATTATGAG TGATCTAGAG 60 TTGATATGAA GTATATGGGA GGATGTGCAA AGGTGATGTG CAAATACTAT GTCATTTTAT 120 AGGGGGGACT TGAGTATCCT TTGTTACCCT CAGGAGATCC TGAAACCAGT CCCCCATGGA 180 TACTGAGGGC TGACTGTATA GTCCTATCCT CACGGAACTT TCATTCTAAT GGGGGAAGAC 240 TGACTATAAA CAAAATATAT GTAATAGGTG GTGGTAAGTA CCGTGGAGAA GTAACAAATG 300 GGGCAAAGTG AGTTATACAG CTCCATTCTT AGAAACCTTG GAGTACTTTT CTTAGTTTAT 360 ACTCGTGGTG GTTTCCTTTT GTCTCCTTTA TTACATGGGA CTCTGACATG TGCCCATAGC 420 TAGGGTGACA GTAGGATCTA CCCGATAGTA GGGTGGCAGT AGGATCTACC CAAAAAGCGT 480 CCTGCTGATA CAGGACCAAA GCATCCTGTT GTTCTCGAGC CTATAAAAAG AGCTAATGGT 540 GTTGCTTCTC TTAACTGTGG CCTCCTACAC TGTGTTTTGG ATGATTGGTG ATGTCTTGGA 600 TATTCTGTTT CTTTGGAACT TTGAATATAC AACACTTTAC TAGGGAATTA GCAATGGAAG 660 CAGAGCAAAG ATGTACAGAG GAAACAATGC GTAACTCTGA TGGAATTGAA GTCATGAGGC 720 AGCAGAGAGC TTAAATTACA GCTTTAAAAA TTTTTATTTT TTAGAGGGAA TTTACTTGGG 780 AGTAACAGCA GTAATAGTTA ACGGAGCCAG AATGCTTGAG TCATATAATT GCAAAGCAGA 840 GTTGGGAGCA ACAGATGCTA AAGAGTAGTT GCTGTAGTTC CTCTTTGGGT CGTAGGAGCA 900 GTTGTCATAT TACTATATAG CTACTGCATG AAGAAGAGTT CTTAGTGAGG CCTGGGTGAA 960 CAGCTCTTCT TAGTATTCTG TGTGACCCCA TTTGACCTTT TAACAAATCC CTAAGTAAAT 1020 AAATAGCCCC TCAGGAAAAC TAAGTTTTTC TCTGCTGTTT TTTTGCTTGA GAGAGCTATA 1080 ACTGTAATAG ACTTATATTT CTGAACATTT TAGTGCTTGC CAATATTTGG TAATATTTAT 1140 GTTTCCTATA TTTGTAATGA ACATTCTTCT TCCGGTACAT TTTTTGTTAA ATTATTGTTT 1200 GATGGATAAA AGTTCACCTT TTATTGTATA AAATTGACTG AGATTAATTT ATACACATTG 1260 ACAATGGGTA AATAGAATTT TTCAGATTAT TAAAAGCTGA AGGATGACCA CGTAAGCAAA 1320 AAAAAAAAAA AAAAAACCAA CAAAAATAAA CCCAAACCCC TCAAACAATT TCGAACACGA 1380 AACATTCTTC TGATGCCGGC ATCCCTGCTT GCAGGTGTGA AGGGGGCAGG AATCAGCGAG 1440 GTGTCCTGGG CTGAGTCCCC GGGGAAGAAT ATGAT Seq ID NO: 2 DNA sequence Nucleic Acid Accession #: X83301.1 1   11   21   31   41   51 |  |   |    |   |   | GCAAAGCCAG CTGGGCTCCT GAGTCCGGTG GGTACTTGGA GAACTTACTA CGTCTAGCTG 60 GAGGATTGTA AATGCACCAA TCAGCATGCT GTGTCTAGCT CAAGATTTTC TCCATCCCCT 120 TATTTTGGGC CAGTGGCTGT CATTACATAT GAGATGAGTC TCTTGAAGAC TACAGATGAA 180 CTCAAGCTCC ATGAGGAGAT GTTTCATTGT CGAGAGCAGT CATGATGGCC TGCACTCCAC 240 ACAATGCAAC AGAGTGAAAG AGCAGGTTCT GCTTCTTTGG TGTAGTCCTG AAGCTTCCTA 300 AGAAACTTCA CATCAGGTGA TGGATAGGAG CAACCCTGTA AAACCAGCCT TAGACTATTT 360 TTCAAACAGG CTGGTGAATT ACCAGATCTC CGTCAAGTGC AGTAACCAGT TCAAGTTGGA 420 AGTGTGTCTT TTGAATGCAG AGAACAAAGT CGTGGACAAC CAGGCTGGGA CCCAGGGCCA 480 GCTGAAGGTG CTGGGTGCCA ACCTCTGGTG GCCGTACCTG ATGCACGAAC ACCCCGCCTA 540 CCTGTACTCC TGGGAGGATG GTGATTGCTC ACACCAAAGC CTTGGACCCC TCCCAGCCTG 600 TGACCTTTGG GACCAACTCC ACCTACGCAG CAGACAAGGG GGCTCTGTAT GTGGATGTGA 660 TCCGTGTGAA CAGCTACTAC TCTTGGTATC GCAACTACGG GCACCTGGAG TTGATTCGGC 720 TGCAGCTGGC CGCCCAGTTT GAGAATTGGT GTGAGACATC ACAATCCCAT TATTCAGAGC 780 GCGTATGGAG TGGAAACGCT TGTAGGGTTT CACCAGGGCT GGTGAATTAC CAGATCTCCG 840 TCAAGTGCAG TAACCAGTTC AAGTTGGAAG TATGTCTTTT GAATGCAGAA AACAAAGTCG 900 TGGACAACCA GGCTGGGACC CAGGGCCAGC TGAAGGTGCT GGTGCCAACC TCTGGTGGCC 960 GTACCTGATG CACGAACACC CCGCCTACCT GTACTCGTGG GAGGATGGTG ATTGCTCACA 1020 CCAAAGCCTT GGACCCCTCC CAGCCTGTGA CCTTTGGGAC CAACTCCACC TACGCAGCAG 1080 ACAAGGGGGC TCTGTATGTG GATGTGATCC GTGTGAACAG CTACTACTCT TGGTATCGCA 1140 ACTACGGGCA CCTGGAGTTG ATTCGGCTGC AGGCCCTGCA GCTGGCCGCC CAGTTTGTGA 1200 ATTGGTGTAA GACATCACAA TCCCATTATT CAGAGCGCGT ATGGAGTGGA AACGCTTGTA 1260 GGGTTTCACC AGTCTTTCCC AGGGAACTCC GATGAAGTGT TCCAACAAAA TGAGCGAGTG 1320 AACCAAGAAG AGGATGACAT TAGATCCAGG AGATACAACA GAGGAGATAA TCTCCAGGAT 1380 GCCTGTGAAG AAAGATCCCT GGATCCCAGG ATGATTATAG GACAAGTTGT TCATAATCCA 1440 GCAGGCCAGA AGACTTCCAG GGAAACTCAT TTCAAGATGA AAATGGACCA GCCGCAGTGG 1500 CTCACGCCTG TAATACCAGC ACTTTGGGAG GCTGAGGCGG GCGGATCACT TGAGGTCAAG 1560 AGTTTGAAAC TAGCCTGGCC AACGTGGCAA AACTCCATCT CTATTAAAGA TACAAAAATT 1620 AGCCAGGCAT AGTGGTGCAT GCCTGTAGTC CCAGCTACTT GGGATGCTGA GGCAGGAAGA 1680 ATTGCTTGAA CCTGGGAGGC AGAGTCTGCG GTGACCGAGA TCATGCCACT GCACTCCAGC 1740 CTGGGTGACA GAGCCAGACT CCGTCTCTAC TAAAAAAAAA AAAAAAAAAA AAA Seq ID NO: 3 Protein sequence: Protein Accession #: CAA58280.1 1   11   21   31   41   51 |  |   |    |   |   | MDRSNPVKPA LDYFSNRLVN YQISVKCSNQ FKLEVCLLNA ENKVVDNQAG TQGQLKVLGA 60 NLWWPYLMHE HPAYLYSWED GDCSHQSLGP LPACDLWDQL HLRSRQGGSV CGCDPCEQLL 120 LLVSQLRAPG VDSAAAGRPV Seq ID NO: 4 DNA sequence Nucleic Acid Accession #: BC002622.1 1   11   21   31   41   51 |  |   |    |   |   | GGCACGAGGC TCCGCCCGCG GCCGGGATGC ACTAGGCAAA GCCAGCTGGG CTCCTGAGTC 60 CGGTGGGTAC TTGGAGAACT TACTACGTCT AGCTGGAGGA TTGTAAATGC ACCAATCAGC 120 ATGCTGTGTC TAGCTCAAGA TTTTCTCCAT CCCCTTATTT TGGGCCAGTG GCTGTCATTA 180 CATATGAGAA CTCAAGCTCC ATGAGGAGAT GTTTCATTGT CGAGAGCAGT CATGATGGCC 240 TGCACTCCAC ACAATGCAAC AGAGTGAAAG AGCAGGTTCT GCTTCTTTGG TGTAGTCCTG 300 AAGCTTCCTA AGAAACTTCA CATCAGGTGA TGGATAGGAG CAACCCTGTA AAACCAGCCT 360 TAGACTATTT TTCAAACAGG CTGGTGAATT ACCAGATCTC CGTCAAGTGC AGTAACCAGT 420 TCAAGTTGGA AGTGTGTCTT TTGAATGCAG AAAACAAAGT CGTGGACAAC CAGGCTGGGA 480 CCCAGGGCCA GCTGAAGGTG CTGGGTGCCA ACCTCTGGTG GCCGTACCTG ATGCACGAAC 540 ACCCCGCCTA CCTGTACTCG TGGGAGGATG GTGATTGCTC ACACCAAAGC CTTGGACCCC 600 TCCCAGCCTG TGACCTTTGT GACCAACTCC ACCTACGCAG CAGACAAGGG GGCTCTGTAT 660 GTGGATGTGA TCCGTGTGAA CAGCTACTAC TCTTGGTATC GCAACTACGG GCACCTGGAG 720 TTGATTCAGC TGCAGCTGGC CGCCCAGTTT GAGAATTGGT GTAAGACATC ACAATCCCAT 780 TATTCAGAGC GCGTATGGAG TGGAAACGCT TGTAGGGTTT CACCAGTCTT TCCCAGGGAA 840 CTCCGATGAA GTGTTCCAAC AAAATGAGCG AGTGAACCAA GAAGAGGATG ACATTAGATC 900 CAGGAGATAC AACAGAGGAG ATAATCTCCA GGATGCCTGT GAAGAAAGAT CCCTGGATCC 960 CAGGATGATT ATAGGACAAG TTGTTCATAA TCCAGCAGGC CAGAAGACTT CCAGGGAAAC 1020 TCATTCAAGG AGGTGAAAAT GATGGATGAC TCCTCCAAGA TGAAAATGGA CCAGCCGCAG 1080 TGGCTCACGC CTGTAATACC AGCACTTTGG GAGGCTGAGG CAGGCGGATC ACTTGAGGTC 1140 AGGAGTTTGA AACTAGCCTG GCCAACGTGG CAAAACTCCA TCTCTATTAA AAATACAAAA 1200 ATTAGCCAAG CATAGTGGTG CATGCCTGTA GTCCCAGCTA CTTGGGATGC TGAGGCAGGA 1260 AGAATTGCTT GAACCTGGGA GGCAGAGTCT ACAGTGAGCC GAGATCATGC CACTGCACTC 1320 CAGCCTGGGC AACACAGTGA GACTCCATCT CAAAAAAAAA AAAAAAAAAA AA Seq ID NO: 5 Protein sequence: Protein Accession #: AAH02622.1 1   11   21   31   41   51 |  |   |    |   |   | MDRSNPVKPA LDYFSNRLVN YQISVKCSNQ FKLEVCLLNA ENKVVDNQAG TQGQLKVLGA 60 NLWWPYLMHE HPAYLYSWED GDCSHQSLGP LPACDLCDQL HLRSRQGGSV CGCDPCEQLL 120 LLVSQLRAPG VDSAAAGRPV Seq ID NO: 6 DNA sequence Nucleic Acid Accession #: see Table 25 & 25A for complete list 1   11   21   31   41   51 |  |   |    |   |   | ACCTGAGATC AGGAGTTCGA GATCAGCCTG ACCAATAGGG TGAAACCCCG TCTCTACTAA 60 AAATACAAAA AATTAGCTGG ACACGATGGT GGGTGCCTGT GGTCCCGGCT ACTCGGGAGG 120 CTGAGACAGG AGAATCAGTT GACCTGGGAG TTGGTGGTTG CAGTGAGCTG AGATCACACC 180 ATTGCATTCC AAGCCTGGGC AACAAGAGTG AAACTCCATC GCAAAAAAAA AAAAGAAGGG 240 GCATAATTTG TGGATGAGGA TTGGATATAA GGTAAAGGAT GGGACATTCT TGGACTTACA 300 GATGGTGTGA TTGCCTGGCT AGAAGAAGAA TTCCCGGTCA AAAAGAAACC ATCAGCTTTC 360 CAAGTGTGAA AGAGAGATAA ATCTGTGAAG ATTATAGGGA CTACAGGAAA CTTAATCTTT 420 TTCTTTGAAA AAGCAATTGT AGCAAAAAAA AAGAAAATTT CTTACTGTCA TCTAAAATTG 480 ACATGGACAT CTTAGTGGAC TAGAAGTTAA GGGCATAAAT TCTCCCAGTG ATTTTTAATT 540 TTAGCATTGT GATTAACACC TTCTAAAATT GCCAGAACTT AATAAATAAT TGCTTTTCAT 600 TATTAGTATG CCATCAAATT TAGTAGCTGT TTCAGGCTTT AATGTGTCAA GCCTAAAATC 660 CAGATTTTTG AGGATCTTCT CCCTCTTAAA AGAGTATTCA GTTAACTGCC GTAGAAATAC 720 ACATGTATAC AAGGGCACTG TATACATCAG TCTAAAAAAT AAAAATATGT ATACGTTCTG 780 GTGAGTCTAG CACAGCATTG CCCAATAGAA ATACCAATGG AGGTCACAAA TGTGGCCCAT 840 ATAGGTTAAT TGGTAAATTT TCTNATAGNC ACC Seq ID NO: 7 DNA sequence Nucleic Acid Accession #: AK000942 Coding sequence: 1204-1503 1   11   21   31   41   51 |  |   |    |   |   | GTAAAGGAAT GTCTTTTTAA TTCAGCTTTT CTTTTCTCCA TGCTAGTGTT ATCAGGTTTT 60 GGTATTTATT TACTTACAGC ATATGTTATG AAGCTGGTTT GAAAATTGGT TTTAGATATA 120 TCTGCAAGTT TACTACTTTG ACTGTAAAAA AAAAAAATGA AAAAGTAGTT GACATCTGTC 180 CTCAGAAGAA GTTTGCAGGT TGCATATTTG TGTGTAAATA CACAGGCTAA AAGGTAATTT 240 ATGTTCCTTG GGAATTGAAA TGGTCAGTGG CCCGTTACAG AAACTTATCA GTCATATATC 300 AGCACCAGTT CATTCTTTTG CACCTTAGGG ACCATCTGTC CCCTGAGGTG ACCTGAGAAA 360 CAACCAGTTG CCCACAGACT GTTATTTCTT CAAGTGAGCC AGGATTTGAT TTCACTGCCT 420 TATATTCTAT TTTTAGTGTA CAGTGCTTTG ATTTTTTGGA AAAACTAAAT TTTAAACATA 480 TTTGAAAAAT GTTATAAGAC TTGGACATTA AGTCTGTTGA TAGCCAAAGT CAGTTTACCA 540 AAGTAAAACA AATAAATTCT ATGCTTCTTC ATTGTCAAAG AGCAGTCTGC CATCATGTGG 600 ATATAAATGG ACTATGTAAA GTGACATGGT GCTTACTCTC TACCTAATAA TAGCCTCCCT 660 CCTGTTCCAA CAAGATAACC AACAGGTATA TTTAATTTAC CAGTTAATAT GTTTTGGATA 720 ATTGGCTGCC TTGAAATGCT ATATGTTTTA TAGTACATCA TAGCTTTAGT TTTCTTCATA 780 AGGAAATTAC AGTTACATCC TGGCTAACAT GGTGAAACTC CATCTCTACT AAAAATACAA 840 AAAATTAGCC GGGCGTGGTG GCGGGCACTT GTAGTCCCAG CTACTCGGGA GGCTGAGGCA 900 GGAGAATGGC GTGAACCCAG GAGGCGGAGG TTGCAGTGAG CCGAGATCGT GCCACTGTAC 960 TCTGGCCTGG GAGACAGAGC GAGACTCCAT CTCAAAAAAA AAAAAAAAAA AAAAAAAAGA 1020 GAGAGAGAGA CCTGGAGTAG AGATTCTGTC AAAGAACTTT TTCTTTCTTG AGAAGCATCT 1080 GAAATGGAAT CTGTTGTCTC TTCGAAATAT GTACTGCTGT AACAGTGAAA CAACCCTCAG 1140 AGTATGCCTT CGTGTGGGCT ACTCGTTGTG GTTTTGAACT TGGGGGAACT GTCTGTGTTT 1200 GGGTCAAGAA TATGCAACTG GCTGGGCACA TTGGCTCACG CCTGTAATCC CAGCAATTTG 1260 GGAGGCTGAG GCAGGCGGAT CACCTGAGGT CAGGGCTTCA AGACCAGACT GGCCAACATG 1320 GTGAAACCCC GTCTCTACTG AAAATACAAA AATTAGCTGG GCATGGTGGC AGGTGCCTGT 1380 AATCCCAGCT ACTCGGGAGG CTGACGTGAG AGAATCGCTT GAACCCGGGA GTTGGAGGTT 1440 GCAGTGAGCC GAGATTGCAC CATTGCACTC CAGCTTGGGC AACAAGAGTG AAACTCTTGT 1500 CTCAG Seq ID NO: 8 DNA sequence Nucleic Acid Accession #: see Table 25 & 25A for complete list 1   11   21   31   41   51 |  |   |    |   |   | GACTAGGCTG GGCAACATAG TGAGACCTCA TCTCTAAAAT TAAAAAAATA AAAGCCACCA 60 GAAAAAAACC TAAAAACATG CCAAGTGACA TCAGTCTTTG ATGAAAATGG CAGCAGAAGA 120 GTGATGCCAT GGGTGGGGGT GGGAAATGCT ATTTCAGCAG AGAGGGAGCT GTCATGGAAG 180 ACACCATGTG GCTGGGCACG GTGGCTCACA CCTGTAATCC CAGCACTTTG GGAGATAGAG 240 GCAGGTGGAT CCCTTGAGCT TAGGAATTTG AGACTAGCCT GGGCAATAAG AGTGAAACTC 300 CATCTCAAAA AAAAAAAAAA AAAAAGGTGC ATGAAACATA TGAAGCAAAA AGTGAAAGTC 360 CCCATTCTTT TCCTTTTTCC AGAGGTGATT TTTGTGGCCA ATCTGGTTTC ATTCCCTCCC 420 AGACACTTTT CTAGGCATCT ATGCGCCTCT ATTCACATAT AAACAAAATA GGAGTTTTCC 480 TGTGCTTCCC TTAAATGGCA TATGTATCTT TCACTCTTTT TTTTCACCTA GTGGATCTTT 540 AATACCTTAA AAGCTCAACC TGGGCTTGGT GCGGTGGCTC ATACGTGTAA TCCCAGGCCT 600 TTGGGAGGCC AAGGTGGGAG GATCACTTGA GCTCAGGAGT TCCAGACCAT TCCAAAGCAA 660 AAACAAAAGG ATTTTGAGAT CAGTGTGGGC AACTTAGCAA AACACCATCT CTTAAAAAAA 720 AAAAAAAAAA Seq ID NO: 9 DNA sequence Nucleic Acid Accession #: BC010433.1 Coding sequence: 3-335 1   11   21   31   41   51 |  |   |    |   |   | GGTCGCCCTC CGTCGTGGTC TGGCGTGTAT TCCGAGCCTT GGTGTCTGGC GGTTTCCGAG 60 CGTTGGTGTC TGGCGGTTTC CGAGCGTTGG TGTCTGGCGG TTTCCGACCG TTGGTGTCTG 120 GCGGTTTCCG ACCGTTGGTG TCTGGCACGC GCCACCCTCT CTTGCTTTGG TTGCGCCATG 180 CCGATGTACC AGACAAGAAG ACAAGAAAAT GATTTGAGGA CAGCTTCAAT CGCGGTGTGA 240 AGAAGAAAGC AGCAAAACGA CCACTGAAAA CAACGCCGGT GGCAAAATAT CCAAAGAAAG 300 GGTCCCAAGC GGTACATCGT CATAGCCGGA AACAGTCAGA GCCACCAGCC AATGATCTTT 360 TCAATGCTGC GAAAGCTGCC AAAAGTGACA TGCAGCACCG AGAAGTCCGC GTGAAGTGCG 420 TGAAGGCTCT GAAAGGGCTG TACGGTAACC GGGACCTGAC CGCACGCCTG GAGCTCTTCA 480 CTGGCCGCTT CAAGGACTGG ATGGTTTCCA TGATCATGGA CAGAGAGTAC AGTGTGGCAG 540 TGGAGGCCGT CAGATTACTG ATACTTATCC TTAAGAACAT GGAAGGGGTG CTGATGGACG 600 TGGACTGTGA GAGCGTCTAC CCCATTGTGT AGGCCTCTAA TTGAGGCCTG GCCTCTGCTG 660 TGGGTGAATT TCTGTACTGG AAACTTTTCT ACCCTGAGTG CGAGATAAGA ACGATGGGTG 720 GAAGAGAGCA ACGCCAGAGC CCAGGTGCCC AGAGGACTTT CTTCCAGCTT CTGCTGTCCT 780 TCTTTGTGGA GAGCAAGCTC CACGACCACG CTGCTTACTT AGTAGACAAC CTGTGGGACT 840 GTGCAGGGAC TCAGCTGAAG GACTGGGAGG GTCTGACAAG CCTGCTGCTG GAGAAGGACC 900 AGAGCACGTG CCACATGGAG CCAGGGCCAG GGACCTTCCA CCTCCTAGGG TGAAACCAGG 960 AGAGATTGCT TGCTTCACTT GTACAAGGCA GGAACGGTGG CATGGGGTGG GGGAAACTTG 1020 GAGTTGGAAG GTGGCTAATC TTTGATTCTA TGTTTTTGAT CCTCCTGGCA CTCCAGACCT 1080 GGGTGATGTG CAGGAGAGCA CACTGATAGA AATCCTTGTG TCCAGTGCCC AGCAACTCCT 1140 GCCTCAGCCT CCCGAGCAGC TGGGACTACA GGCGCCCGCC ACCACGCCTG GCTAACTTTT 1200 TTGTGTTTTT AGTAGAGACG GGTTTTCACC GTGTTGGCCA GGATGGTCTT GATCTCTTGA 1260 CCTTGTGATC CACCTGCCTC ATCATCCCAA AGTGCTGGGA TTACAGGCGT GAGCCACTGC 1320 GCCCAGCATG TTAGACAATT TTTAATTCAT CCTCTCTGTG CTGTTGTTTT CTCAGCTGTG 1380 AAAGGAATAT TCTGGTGGGG ACAAGGTTAC AGAGTTGCTG AGAGGGTCTC ATGACATGAA 1440 GGTACTGGCC TTGGCACAGT GCCTGGGGGG GCGGGGACTC CGCACATGCC TGTGATGTCA 1500 CAGTTACTGT CAGTTCACAG CGAACCTTCC CTCCTTTTCC TGTTGACTTT CCCACACTCC 1560 TGTAACCCTC CCTCCCTCCC TTCTTCCTCT CTCTCTCTCT CACTCACGCA CACGCACACA 1620 CACACACACA CACACACACA CACACACTCC ATTCACTGTC TCCATGACTC TGGAGTAAAC 1680 TAACGTCTCG AGTFGCCATT GGAAGCCCCG TTGTCCTCAT TTAGACTTTC ATGGGTTATA 1740 GGCACTTTTG ACTTCCTGGG GTCCTTCTTC AGTTAAAAAA AAAAATTAGA AAATTAGGCC 1800 GGGCGTGGTG GCACATGCCT GTAATCCCAG CACCTTGGCC TCCCAAAGTG CTGGGATTAC 1860 AGGAGTGAGC CACCATGCCC AGCCTCCGTT GTCCTCATTT AGACTTTCAT GGGTTATAGG 1920 CACTTTTGAC TTCCTGGGGT CCTTCTTCAG TTAAAAAAAA AAAAAAAAAA Seq ID NO: 10 DNA sequence Nucleic Acid Accession #: see Table 25 & 25A for complete list 1   11   21   31   41   51 |  |   |    |   |   | AGTGGNTCCC CCGGNCTGCA GGAATTCGGC ACGAGATCAT GATGGCTAAT ATTTCCTGAG 60 CACCTTTCAT TCAGGCATGA TGCCAGGTGC ACCAACTTAC TTAATCCTCA TAGCCACCAC 120 CTGAGCAAGC TCCTGTTTTA TAAATGGACC AGTTCTTGTT GCTGTTGTAC AAGTTATTTT 180 CTTTCTATAA CGTCCTCCTT GTCCTCCTTC CACATTCTTA AAGAAACTTT CCCTTCCTTT 240 AAAGTACTCA GGGAGCCCTG CATTGCTTCT TGAAGCCTTC TCCAGCTTCA TCATCTCACA 300 GTGGTCTCTC TTETCACTAA ATGTCCAATA TGCTGCACAT AAGTACCCCA AAGTTAGCAC 360 AGGAATTGTT CCATGGCTGT CATATATGTT AAAAATCATT AAAAGTTCAT TTTTTCTCTC 420 ATTATGGGAA GGATACATGC TCCTACTAGT AAATTTAGTA GGTAGAAAAA AATTATCACT 480 ATCTAGACTG CTTTCCATTT AGTCTTTATG CATAGCTTTC GTGTCTGCCT ATTTTTACCT 540 TGTGTTTGTA ACTTACTATT ATAAAATATG CGTCTCTATG TTCATTGTCA ACGATTATTT 600 ACAATAACAT GGAGTGGATT TACATGTATT CTCTATATTT GGATTAAAGG AGATAGAGTA 660 TGTGAAATTA AATGGGAGAA GTATCTGATA CATAACAGGC AATACAAATA TTATCACATA 720 GCGTCAATTT ATTTGTGAAT ATTGAAAGCT CCAAAAAAGA AAAAAAGTTT TTTTTTAATT 780 CCCGTAATTA CTTATTGCAG TATTGTGTTC ATACAAACTG CTCAGTCATT TTGGAGAAAT 840 AACAATTTTT TTCCTCATCA TGAAGTAAGG TATGCTCACT GCAAAAAAAA TCTAGAAAAT 900 AAAGAGGAAC ATGCTAAAGA AAAGAATACT CCCATATAAT CTCTGTCTTC ATAAATAATC 960 TTTTGTAACG CTTATACACT GCTGGTGGGA ATGTAAATTA GTTCAGCCAT TGTGAAAAGT 1020 AGCGTAGCAA TTCCTTGAAA AACTTAAAAT AGATTTACCG TTCAACCCAG CAATCCCATT 1080 ATTGGGCATA TACCCAGTGG AATGTAAATC ATCCTGCCAT AAAAACACAT GCACATGTAT 1140 GTTCATTGCA GCACTATTCA CAATAGCAAA GACATGGAAT CAACCTATAT GCCCATCAAT 1200 AGTAGACTGA ATAAAGAAAA TATGGTACAT ATTCACCACA GAATACTAAG CAGCCATAAA 1260 AAAAAA Seq ID NO: 11 DNA sequence Nucleic Acid Accession #: NM_000582.1 Coding sequence: 88-990 1   11   21   31   41   51 |  |   |    |   |   | GCAGAGCACA GCATCGTCGG GACCAGACTC GTCTCAGGCC AGTTGCAGCC TTCTCAGCCA 60 AACGCCGACC AAGGAAAACT CACTACCATG AGAATTGCAG TGATTTGCTT TTGCCTCCTA 120 GGCATCACCT GTGCCATACC AGTTAAACAG GCTGATTCTG GAAGTTCTGA GGAAAAGCAG 180 CTTTACAACA AATACCCAGA TGCTGTGGCC ACATGGCTAA ACCCTGACCC ATCTCAGAAG 240 CAGAATCTCC TAGCCCCACA GACCCTTCCA AGTAAGTCCA ACGAAAGCCA TGACCACATG 300 GATGATATGG ATGATGAAGA TGATGATGAC CATGTGGACA GCCAGGACTC CATTGACTCG 360 AACGACTCTG ATGATGTAGA TGACACTGAT GATTCTCACC AGTCTGATGA GTCTCACCAT 420 TCTGATGAAT CTGATGAACT GGTCACTGAT TTTCCCACGG ACCTGCCAGC AACCGAAGTT 480 TTCACTCCAG TTGTCCCCAC AGTAGACACA TATGATGGCC GAGGTGATAG TGTGGTTTAT 540 GGACTGAGGT CAAAATCTAA GAAGTTTCGC AGACCTGACA TCCAGTACCC TGATGCTACA 600 GACGAGGACA TCACCTCACA CATGGAAAGC GAGGAGTTGA ATGGTGCATA CAAGGCCATC 660 CCCGTTGCCC AGGACCTGAA CGCGCCTTCT GATTGGGACA GCCGTGGGAA GGACAGTTAT 720 GAAACGAGTC AGCTGGATGA CCAGAGTGCT GAAACCCACA GCCACAAGCA GTCCAGATTA 780 TATAAGCGGA AAGCCAATGA TGAGAGCAAT GAGCATTCCG ATGTGATTGA TAGTCAGGAA 840 CTTTCCAAAG TCAGCCGTGA ATTCCACAGC CATGAATTTC ACAGCCATGA AGATATGCTG 900 GTTGTAGACC CCAAAAGTAA GGAAGAAGAT AAACACCTGA AATTTCGTAT TTCTCATGAA 960 TTAGATAGTG CATCTTCTGA GGTCAATTAA AAGGAGAAAA AATACAATTT CTCACTTTGC 1020 ATTTAGTCAA AAGAAAAAAT GCTTTATAGC AAAATGAAAG AGAACATGAA ATGCTTCTTT 1080 CTCAGTTTAT TGGTTGAATG TGTATCTATT TGAGTCTGGA AATAACTAAT GTGTTTGATA 1140 ATTAGTTTAG TTTGTGGCTT CATGGAAACT CCCTGTAAAC TAAAAGCTTC AGGGTTATGT 1200 CTATGTTCAT TCTATAGAAG AAATGCAAAC TATCACTGTA TTTTAATATT TGTTATTCTC 1260 TCATGAATAG AAATTTATGT AGAAGCAAAC AAAATACTTT TACCCACTTA AAAAGAGAAT 1320 ATAACATTTT ATGTCACTAT AATCTTTTGT TTTTTAAGTT AGTGTATATT TTGTTGTGAT 1380 TATCTTTTTG TGGTGTGAAT AAATCTTTTA TCTTGAATGT AATAAGAATT TGGTGGTGTC 1440 AATTGCTTAT TTGTTTTCCC ACGGTTGTCC AGCAATTAAT AAAACATAAC CTTTTTTACT 1500 GCCTAAAAAA AAAAAAAAAA AAAA Seq ID NO: 12 Protein sequence: Protein Accession #: NP_000573.1 1   11   21   31   41   51 |  |   |    |   |   | MRIAVICFCL LGITCAIPVK QADSGSSEEK QLYNKYPDAV ATWLNPDPSQ KQNLLAPQTL 60 PSKSNESHDH MDDMDDEDDD DHVDSQDSID SNDSDDVDDT DDSHQSDESH HSDESDELVT 120 DFPTDLPATE VFTPVVPTVD TYDGRGDSVV YGLRSKSKKF RRPDIQYPDA TDEDITSHME 180 SEELNGAYKA IPVAQDLNAP SDWDSRGKDS YETSQLDDQS AETHSHKQSR LYKRKANDES 240 NEHSDVIDSQ ELSKVSREFH SHEFHSHEDM LVVDPKSKEE DKHLKFRISH ELDSASSEVN Seq ID NO: 13 DNA sequence Nucleic Acid Accession #: NM_001793 Coding sequence: 71-2560 1   11   21   31   41   51 |  |   |    |   |   | AAAGGGGCAA GAGCTGAGCG GAACACCGGC CCGCCGTCGC GGCAGCTGCT TCACCCCTCT 60 CTCTGCAGCC ATGGGGCTCC CTCGTGGACC TCTCGCGTCT CTCCTCCTTC TCCAGGTTTG 120 CTGGCTGCAG TGCGCGGCCT CCGAGCCGTG CCGGGCGGTC TTCAGGGAGG CTGAAGTGAC 180 CTTGGAGGCG GGAGGCGCGG AGCAGGAGCC CGGCCAGGCG CTGGGGAAAG TATTCATGGG 240 CTGCCCTGGG CAAGAGCCAG CTCTGTTTAG CACTGATAAT GATGACTTCA CTGTGCGGAA 300 TGGCGAGACA GTCCAGGAAA GAAGGTCACT GAAGGAAAGG AATCCATTGA AGATCTTCCC 360 ATCCAAACGT ATCTTACGAA GACACAAGAG AGATTGGGTG GTTGCTCCAA TATCTGTCCC 420 TGAAAATGGC AAGGGTCCCT TCCCCCAGAG ACTGAATCAG CTCAAGTCTA ATAAAGATAG 480 AGACACCAAG ATTTTCTACA GCATCACGGG GCCGGGGGCA GACAGCCCCC CTGAGGGTGT 540 CTTCGCTGTA GAGAAGGAGA CAGGCTGGTT GTTGTTGAAT AAGCCACTGG ACCGGGAGGA 600 GATTGCCAAG TATGAGCTCT TTGGCCACGC TGTGTCAGAG AATGGTGCCT CAGTGGAGGA 660 CCCCATGAAC ATCTCCATCA TCGTGACCGA CCAGAATGAC CACAAGCCCA AGTTTACCCA 720 GGACACCTTC CGAGGGAGTG TCTTAGAGGG AGTCCTACCA GGTACTTCTG TGATGCAGGT 780 GACAGCCACG GATGAGGATG ATGCCATCTA CACCTACAAT GGGGTGGTTG CTTACTCCAT 840 CCATAGCCAA GAACCAAAGG ACCCACACGA CCTCATGTTC ACCATTCACC GGAGCACAGG 900 CACCATCAGC GTCATCTCCA GTGGCCTGGA CCGGGAAAAA GTCCCTGAGT ACACACTGAC 960 CATCCAGGCC ACAGACATGG ATGGGGACGG CTCCACCACC ACGGCAGTGG CAGTAGTGGA 1020 GATCCTTGAT GCCAATGACA ATGCTCCCAT GTTTGACCCC CAGAAGTACG AGGCCCATGT 1080 GCCTGAGAAT GCAGTGGGCC ATGAGGTGCA GAGGCTGACG GTCACTGATC TGGACGCCCC 1140 CAACTCACCA GCGTGGCGTG CCACCTACCT TATCATGGGC GGTGACGACG GGGACCATTT 1200 TACCATCACC ACCCACCCTG AGAGCAACCA GGGCATCCTG ACAACCAGGA AGGGTTTGGA 1260 TTTTGAGGCC AAAAACCAGC ACACCCTGTA CGTTGAAGTG ACCAACGAGG CCCCTTTTGT 1320 GCTGAAGCTC CCAACCTCCA CAGCCACCAT AGTGGTCCAC GTGGAGGATG TGAATGAGGC 1380 ACCTGTGTTT GTCCCACCCT CCAAAGTCGT TGAGGTCCAG GAGGGCATCC CCACTGGGGA 1440 GCCTGTGTGT GTCTACACTG CAGAAGACCC TGACAAGGAG AATCAAAAGA TCAGCTACCG 1500 CATCCTGAGA GACCCAGCAG GGTGGCTAGC CATGGACCCA GACAGTGGGC AGGTCACAGC 1560 TGTGGGCACC CTCGACCGTG AGGATGAGCA GTTTGTGAGG AACAACATCT ATGAAGTCAT 1620 GGTCTTGGCC ATGGACAATG GAAGCCCTCC CACCACTGGC ACGGGAACCC TTCTGCTAAC 1680 ACTGATTGAT GTCAATGACC ATGGCCCAGT CCCTGAGCCC CGTCAGATCA CCATCTGCAA 1740 CCAAAGCCCT GTGCGCCAGG TGCTGAACAT CACGGACAAG GACCTGTCTC CCCACACCTC 1800 CCCTTTCCAG GCCCAGCTCA CAGATGACTC AGACATCTAC TGGACGGCAG AGGTCAACGA 1860 GGAAGGTGAC ACAGTGGTCT TGTCCCTGAA GAAGTTCCTG AAGCAGGATA CATATGACGT 1920 GCACCTTTCT CTGTCTGACC ATGGCAACAA AGAGCAGCTG ACGGTGATCA GGGCCACTGT 1980 GTGCGACTGC CATGGCCATG TCGAAACCTG CCCTGGACCC TGGAAGGGAG GTTTCATCCT 2040 CCCTGTGCTG GGGGCTGTCC TGGCTCTGCT GTTCCTCCTG CTGGTGCTGC TTTTGTTGGT 2100 GAGAAAGAAG CGGAAGATCA AGGAGCCCCT CCTACTCCCA GAAGATGACA CCCGTGACAA 2160 CGTCTTCTAC TATGGCGAAG AGGGGGGTGG CGAAGAGGAC CAGGACTATG ACATCACCCA 2220 GCTCCACCGA GGTCTGGAGG CCAGGCCGGA GGTGGTTCTC CGCAATGACG TGGCACCAAC 2280 CATCATCCCG ACACCCATGT ACCGTCCTCG GCCAGCCAAC CCAGATGAAA TCGGCAACTT 2340 TATAATTGAG AACCTGAAGG CGGCTAACAC AGACCCCACA GCCCCGCCCT ACGACACCCT 2400 CTTGGTGTTC GACTATGAGG GCAGCGGCTC CGACGCCGCG TCCCTGAGCT CCCTCACCTC 2460 CTCCGCCTCC GACCAAGACC AAGATTACGA TTATCTGAAC GAGTGGGGCA GCCGCTTCAA 2520 GAAGCTGGCA GACATGTACG GTGGCGGGGA GGACGACTAG GCGGCCTGCC TGCAGGGCTG 2580 GGGACCAAAC GTCAGGCCAC AGAGCATCTC CAAGGGGTCT CAGTTCCCCC TTCAGCTGAG 2640 GACTTCGGAG CTTGTCAGGA AGTGGCCGTA GCAACTTGGC GGAGACAGGC TATGAGTCTG 2700 ACGTTAGAGT GGTTGCTTCC TTAGCCTTTC AGGATGGAGG AATGTGGGCA GTTTGACTTC 2760 AGCACTGAAA ACCTCTCCAC CTGGGCCAGG GTTGCCTCAG AGGCCAAGTT TCCAGAAGCC 2820 TCTTACCTGC CGTAAAATGC TCAACCCTGT GTCCTGGGCC TGGGCCTGCT GTGACTGACC 2880 TACAGTGGAC TTTCTCTCTG GAATGGAACC TTCTTAGGCC TCCTGGTGCA ACTTAATTTT 2940 TTTTTTTAAT GCTATCTTCA AAACGTTAGA GAAAGTTCTT CAAAAGTGCA GCCCAGAGCT 3000 GCTGGGCCCA CTGGCCGTCC TGCATTTCTG GTTTCCAGAC CCCAATGCCT CCCATTCGGA 3060 TGGATCTCTG CGTTTTTATA CTGAGTGTGC CTAGGTTGCC CCTTATTTTT TATTTTCCCT 3120 GTTGCGTTGC TATAGATGAA GGGTGAGGAC AATCGTGTAT ATGTACTAGA ACTTTTTTAT 3180 TAAAGAAACT TTTCCCAGAA AAAAA Seq ID NO: 14 Protein sequence: Protein Accession #: NP_001784.2 1   11   21   31   41   51 |  |   |    |   |   | MGLPRGPLAS LLLLQVCWLQ CAASEPCRAV FREAEVTLEA GGAEQEPGQA LGKVFMGCPG 60 QEPALFSTDN DDFTVRNGET VQERRSLKER NPLKIFPSKR ILRRHKRDWV VAPISVPENG 120 KGPFPQRLNQ LKSNKDRDTK IFYSITGPGA DSPPEGVFAV EKETGWLLLN KPLDREEIAK 180 YELFGHAVSE NGASVEDPMN ISIIVTDQND HKPKFTQDTF RGSVLEGVLP GTSVMQVTAT 240 DEDDAIYTYN GVVAYSIHSQ EPKDPHDLMF TIHRSTGTIS VISSGLDREK VPEYTLTIQA 300 TDMDGDGSTT TAVAVVEILD ANDNAPMFDP QKYEAHVPEN AVGHEVQRLT VTDLDAPNSP 360 AWRATYLIMG GDDGDHFTIT THPESNQGIL TTRKGLDFEA KNQHTLYVEV TNEAPFVLKL 420 PTSTATIVVH VEDVNEAPVF VPPSKVVEVQ EGIPTGEPVC VYTAEDPDKE NQKISYRILR 480 DPAGWLAMDP DSGQVTAVGT LDREDEQFVR NNIYEVMVLA MDNGSPPTTG TGTLLLTLID 540 VNDHGPVPEP RQITICNQSP VRQVLNITDK DLSPHTSPFQ AQLTDDSDIY WTAEVNEEGD 600 TVVLSLKKFL KQDTYDVHLS LSDHGNKEQL TVIRATVCDC HGHVETCPGP WKGGFILPVL 660 GAVLALLFLL LVLLLLVRKK RKIKEPLLLP EDDTRDNVFY YGEEGGGEED QDYDITQLHR 720 GLEARPEVYL RNDVAPTIIP TPMYRPRPAN PDEIGNFIIE NLKAANTDPT APPYDTLLVF 780 DYEGSGSDAA SLSSLTSSAS DQDQDYDYLN EWGSRFKKLA DMYGGGEDD Seq ID NO: 15 DNA sequence Nucleic Acid Accession #: XM_051860.2 Coding sequence: 261-4346 1   11   21   31   41   51 |  |   |    |   |   | GAGCTAGCGC TCAAGCAGAG CCCAGCGCGG TGCTATCGGA CAGAGCCTGG CGAGCGCAAG 60 CGGCGCGGGG AGCCAGCGGG GCTGAGCGCG GCCAGGGTCT GAACCCAGAT TTCCCAGACT 120 AGCTACCACT CCGCTTGCCC ACGCCCCGGG AGCTCGCGGC GCCTGGCGGT CAGCGACCAG 180 ACGTCCGGGG CCGCTGCGCT CCTGGCCCGC GAGGCGTGAC ACTGTCTCGG CTACAGACCC 240 AGAGGGAGCA CACTGCCAGG ATGGGAGCTG CTGGGAGGCA GGACTTCCTC TTCAAGGCCA 300 TGCTGACCAT CAGCTGGCTC ACTCTGACCT GCTTCCCTGG GGCCACATCC ACAGTGGCTG 360 CTGGGTGCCC TGACCAGAGC CCTGAGTTGC AACCCTGGAA CCCTGGCCAT GACCAAGACC 420 ACCATGTGCA TATCGGCCAG GGCAAGACAC TGCTGCTCAC CTCTTCTGCC ACGGTCTATT 480 CCATCCACAT CTCAGAGGGA GGCAAGCTGG TCATTAAAGA CCACGACGAG CCGATTGTTT 540 TGCGAACCCG GCACATCCTG ATTGACAACG GAGGAGAGCT GCATGCTGGG AGTGCCCTCT 600 GCCCTTTCCA GGGCAATTTC ACCATCATTT TGTATGGAAG GGCTGATGAA GGTATTCAGC 660 CGGATCCTTA CTATGGTCTG AAGTACATTG GGGTTGGTAA AGGAGGCGCT CTTGAGTTGC 720 ATGGACAGAA AAAGCTCTCC TGGACATTTC TGAACAAGAC CCTTCACCCA GGTGGCATGG 780 CAGAAGGAGG CTATTTTTTT GAAAGGAGCT GGGGCCACCG TGGAGTTATT GTTCATGTCA 840 TCGACCCCAA ATCAGGCACA GTCATCCATT CTGACCGGTT TGACACCTAT AGATCCAAGA 900 AAGAGAGTGA ACGTCTGGTC CAGTATTTGA ACGCGGTGCC CGATGGCAGG ATCCTTTCTG 960 TTGCAGTGAA TGATGAAGGT TCTCGAAATC TGGATGACAT GGCCAGGAAG GCGATGACCA 1020 AATTGGGAAG CAAACACTTC CTGCACCTTG GATTTAGACA CCCTTGGAGT TTTCTAACTG 1080 TGAAAGGAAA TCCATCATCT TCAGTGGAAG ACCATATTGA ATATCATGGA CATCGAGGCT 1140 CTGCTGCTGC CCGGGTATTC AAATTGTTCC AGACAGAGCA TGGCGAATAT TTCAATGTTT 1200 CTTTGTCCAG TGAGTGGGTT CAAGACGTGG AGTGGACGGA GTGGTTCGAT CATGATAAAG 1260 TATCTCAGAC TAAAGGTGGG GAGAAAATTT CAGACCTCTG GAAAGCTCAC CCAGGAAAAA 1320 TATGCAATCG TCCCATTGAT ATACAGGCCA CTACAATGGA TGGAGTTAAC CTCAGCACCG 1380 AGGTTGTCTA CAAAAAAGGC CAGGATTATA GGTTTGCTTG CTACGACCGG GGCAGAGCCT 1440 GCCGGAGCTA CCGTGTACGG TTCCTCTGTG GGAAGCCTGT GAGGCCCAAA CTCACAGTCA 1500 CCATTGACAC CAATGTGAAC AGCACCATTC TGAACTTGGA GGATAATGTA CAGTCATGGA 1560 AACCTGGAGA TACCCTGGTC ATTGCCAGTA CTGATTACTC CATGTACCAG GCAGAAGAGT 1620 TCCAGGTGCT TCCCTGCAGA TCCTGCGCCC CCAACCAGGT CAAAGTGGCA GGGAAACCAA 1680 TGTACCTGCA CATCGGGGAG GAGATAGACG GCGTGGACAT GCGGGCGGAG GTTGGGCTTC 1740 TGAGCCGGAA CATCATAGTG ATGGGGGAGA TGGAGGACAA ATGCTACCCC TACAGAAACC 1800 ACATCTGCAA TTTCTTTGAC TTCGATACCT TTGGGGGCCA CATCAAGTTT GCTCTGGGAT 1860 TTAAGGCAGC ACACTTGGAG GGCACGGAGC TGAAGCATAT GGGACAGCAG CTGGTGGGTC 1920 AGTACCCGAT TCACTTCCAC CTGGCCGGTG ATGTAGACGA AAGGGGAGGT TATGACCCAC 1980 CCACATACAT CAGGGACCTC TCCATCCATC ATACATTCTC TCGCTGCGTC ACAGTCCATG 2040 GCTCCAATGG CTTGTTGATC AAGGACGTTG TGGGCTATAA CTCTTTGGGC CACTGCTTCT 2100 TCACGGAAGA TGGGCCGGAG GAACGCAACA CTTTTGACCA CTGTCTTGGC CTCCTTGTCA 2160 AGTCTGGAAC CCTCCTCCCC TCGGACCGTG ACAGCAAGAT GTGCAAGATG ATCACAGAGG 2220 ACTCCTACCC GGGGTACATC CCCAAGCCCA GGCAAGACTG CAATGCTGTG TCCACCTTCT 2280 GGATGGCCAA TCCCAACAAC AACCTCATCA ACTGTGCCGC TGCAGGATCT GAGGAAACTG 2340 GATTTTGGTT TATTTTTCAC CACGTACCAA CGGGCCCCTC CGTGGGAATG TACTCCCCAG 2400 GTTATTCAGA GCACATTCCA CTGGGAAAAT TCTATAACAA CCGAGCACAT TCCAACTACC 2460 GGGCTGGCAT GATCATAGAC AACGGAGTCA AAACCACCGA GGCCTCTGCC AAGGACAAGC 2520 GGCCGTTCCT CTCAATCATC TCTGCCAGAT ACAGCCCTCA CCAGGACGCC GACCCGCTGA 2580 AGCCCCGGGA GCCGGCCATC ATCAGACACT TCATTGCCTA CAAGAACCAG GACCACGGGG 2640 CCTGGCTGCG CGGCGGGGAT GTGTGGCTGG ACAGCTGCCG GTTTGCTGAC AATGGCATTG 2700 GCCTGACCCT GGCCAGTGGT GGAACCTTCC CGTATGACGA CGGCTCCAAG CAAGAGATAA 2760 AGAACAGCTT GTTTGTTGGC GAGAGTGGCA ACGTGGGGAC GGAAATGATG GACAATAGGA 2820 TCTGGGGCCC TGGCGGCTTG GACCATAGCG GAAGGACCCT CCCTATAGGC CAGAATTTTC 2880 CAATTAGAGG AATTCAGTTA TATGATGGCC CCATCAACAT CCAAAACTGC ACTTTCCGAA 2940 AGTTTGTGGC CCTGGAGGGC CGGCACACCA GCGCCCTGGC CTTCCGCCTG AATAATGCCT 3000 GGCAGAGCTG CCCCCATAAC AACGTGACCG GCATTGCCTT TGAGGACGTT CCGATTACTT 3060 CCAGAGTGTT CTTCGGAGAG CCTGGGCCCT GGTTCAACCA GCTGGACATG GATGGGGATA 3120 AGACATCTGT GYTCCATGAC GTCGACGGCT CCGTGTCCGA GTACCCTGGC TCCTACCTCA 3180 CGAAGAATGA CAACTGGCTG GTCCGGCACC CAGACTGCAT CAATGTTCCC GACTGGAGAG 3240 GGGCCATTTG CAGTGGGTGC TATGCACAGA TGTACATTCA AGCCTACAAG ACCAGTAACC 3300 TGCGAATGAA GATCATCAAG AATGACTTCC CCAGCCACCC TCTTTACCTG GAGGGGGCGC 3360 TCACCAGGAG CACCCATTAC CAGCAATACC AACCGGTTGT CACCCTGCAG AAGGGCTACA 3420 CCATCCACTG GGACCAGACG GCCCCCGCCG AACTCGCCAT CTGGCTCATC AACTTCAACA 3480 AGGGCGACTG GATCCGAGTG GGGCTCTGCT ACCCGCGAGG CACCACATTC TCCATCCTCT 3540 CGGATGTTCA CAATCGCCTG CTGAAGCAAA CGTCCAAGAC GGGCGTCTTC GTGAGGACCT 3600 TGCAGATGGA CAAAGTGGAG CAGAGCTACC CTGGCAGGAG CCACTACTAC TGGGACGAGG 3660 ACTCAGGGCT GTTGTTCCTG AAGCTGAAAG CTCAGAACGA GAGAGAGAAG TTTGCTTTCT 3720 GCTCCATGAA AGGCTGTGAG AGGATAAAGA TTAAAGCTCT GATTCCAAAG AACGCAGGCG 3780 TCAGTGACTG CACAGCCACA GCTTACCCCA AGTTCACCGA GAGGGCTGTC GTAGACGTGC 3840 CGATGCCCAA GAAGCTCTTT GGTTCTCAGC TGAAAACAAA GGACCATTTC TTGGAGGTGA 3900 AGATGGAGAG TTCCAAGCAG CACTTCTTCC ACCTCTGGAA CGACTTCGCT TACATTGAAG 3960 TGGATGGGAA GAAGTACCCC AGTTCGGAGG ATGGCATCCA GGTGGTGGTG ATTGACGGGA 4020 ACCAAGGGCG CGTGGTGAGC CACACGAGCT TCAGGAACTC CATTCTGCAA GGCATACCAT 4080 GGCAGCTTTT CAACTATGTG GCGACCATCC CTGACAATTC CATAGTGCTT ATGGCATCAA 4140 AGGGAAGATA CGTCTCCAGA GGCCCATGGA CCAGAGTGCT GGAAAAGCTT GGGGCAGACA 4200 GGGGTCTCAA GTTGAAAGAG CAAATGGCAT TCGTTGGCTT CAAAGGCAGC TTCCGGCCCA 4260 TCTGGGTGAC ACTGGACACT GAGGATCACA AAGCCAAAAT CTTCCAAGTT GTGCCCATCC 4320 CTGTGGTGAA GAAGAAGAAG TTGTGAGGAC AGCTGCCGCC CGGTGCCACC TCGTGGTAGA 4380 CTATGACGGT GACTCTTGGC AGCAGACCAG TGGGGGATGG CTGGGTCCCC CAGCCCCTGC 4440 CAGCAGCTGC CTGGGAAGGC CGTGTTTCAG CCCTGATGGG CCAAGGGAAG GCTATCAGAG 4500 ACCCTGGTGC TGCCACCTGC CCCTACTCAA GTGTCTACCT GGAGCCCCTG GGGCGGTGCT 4560 GGCCAATGCT GGAAACATTC ACTTTCCTGC AGCCTCTTGG GTGCTTCTCT CCTATCTGTG 4620 CCTCTTCAGT GGGGGTTTGG GGACCATATC AGGAGACCTG GGTTGTGCTG ACAGCAAAGA 4680 TCCACTTTGG CAGGAGCCCT GACCCAGCTA GGAGGTAGTC TGGAGGGCTG GTCATTCACA 4740 GATCCCCATG GTCTTCAGCA GACAAGTGAG GGTGGTAAAT GTAGGAGAAA GAGCCTTGGC 4800 CTTAAGGAAA TCTTTACTCC TGTAAGCAAG AGCCAACCTC ACAGGATTAG GAGCTGGGGT 4860 AGAACTGGCT ATCCTTGGGG AAGAGGCAAG CCCTGCCTCT GGCCGTGTCC ACCTTTCAGG 4920 AGACTTTGAG TGGCAGGTTT GGACTTGGAC TAGATGACTC TCAAAGGCCC TTTTAGTTCT 4980 GAGATTCCAG AAATCTGCTG CATTTCACAT GGTACCTGGA ACCCAACAGT TCATGGATAT 5040 CCACTGATAT CCATGATGCT GGGTGCCCCA GCGCACACGG GATGGAGAGG TGAGAACTAA 5100 TGCCTAGCTT GAGGGGTCTG CAGTCCAGTA GGGCAGGCAG TCAGGTCCAT GTGCACTGCA 5160 ATGCCAGGTG GAGAAATCAC AGAGAGGTAA AATGGAGGCC AGTGCCATTT CAGAGGGGAG 5220 GCTCAGGAAG GCTTCTTGCT TACAGGAATG AAGGCTGGGG GCATTTTGCT GGGGGGAGAT 5280 GAGGCAGCCT CTGGAATGGC TCAGGGATTC AGCCCTCCCT GCCGCTGCCT GCTGAAGCTG 5340 GTGACTACGG GGTCGCCCTT TGCTCACGTC TCTCTGGCCC ACTCATGATG GAGAAGTGTG 5400 GTCAGAGGGG AGCAATGGGC TTTGCTGCTT ATGAGCACAG AGGAATTCAG TCCCCAGGCA 5460 GCCCTGCCTC TGACTCCAAG AGGGTGAAGT CCACAGAAGT GAGCTCCTGC CTTAGGGCCT 5520 CATTTGCTCT TCATCCAGGG AACTGAGCAC AGGGGGCCTC CAGGAGACCC TAGATGTGCT 5580 CGTACTCCCT CGGCCTGGGA TTTCAGAGCT GGAAATATAG AAAATATCTA GCCCAAAGCC 5640 TTCATTTTAA CAGATGGGGA AAGTGAGCCC CCAAGATGGG AAAGAACCAC ACAGCTAAGG 5700 GAGGGCCTGG GGAGCCCCAC CCTAGCCCTT GCTGCCACAC CACATTGCCT CAACAACCGG 5760 CCCCAGAGTG CCCAGGCACT CCTGAGGTAG CTTCTGGAAA TGGGGACAAG TCCCCTCGAA 5820 GGAAAGGAAA TGACTAGAGT AGAATGACAG CTAGCAGATC TCTTCCCTCC TGCTCCCAGC 5880 GCACACAAAC CCGCCCTCCC CTTGGTGTTG GCGGTCCCTG TGGCCTTCAC TTTGTTCACT 5940 ACCTGTCAGC CCAGCCTGGG TGCACAGTAG CTGCAACTCC CCATTGGTGC TACCTGGCTC 6000 TCCTGTCTCT GCAGCTCTAC AGGTGAGGCC CAGCAGAGGG AGTAGGGCTC GCCATGTTTC 6060 TGGTGAGCCA ATTTGGCTGA TCTTGGGTGT CTGAACAGCT ATTGGGTCCA CCCCAGTCCC 6120 TTTCAGCTGC TGCTTAATGC CCTGCTCTCT CCCTGGCCCA CCTTATAGAG AGCCCAAAGA 6180 GCTCCTGTAA GAGGGAGAAC TCTATCTGTG GTTTATAATC TTGCACGAGG CACCAGAGTC 6240 TCCCTGGGTC TTGTGATGAA CTACATTTAT CCCCTTTCCT GCCCCAACCA CAAACTCTTT 6300 CCTTCAAAGA GGGCCTGCCT GGCTCCCTCC ACCCAACTGC ACCCATGAGA CTCGGTCCAA 6360 GAGTCCATTC CCCAGGTGGG AGCCAACTGT CAGGGAGGTC TTTCCCACCA AACATCTTTC 6420 AGCTGCTGGG AGGTGACCAT AGGGCTCTGC TTTTAAAGAT ATGGCTGCTT CAAAGGCCAG 6480 AGTCACAGGA AGGACTTCTT CCAGGGAGAT TAGTGGTGAT GGAGAGGAGA GTTAAAATGA 6540 CCTCATGTCC TTCTTGTCCA CGGTTTTGTT GAGTTTTCAC TCTTCTAATG CAAGGGTCTC 6600 ACACTGTGAA CCACTTAGGA TGTGATCACT TTCAGGTGGC CAGGAATGTT GAATGTCTTT 6660 GGCTCAGTTC ATTTAAAAAA GATATCTATT TGAAAGTTCT CAGAGTTGTA CATATGTTTC 6720 ACAGTACAGG ATCTGTACAT AAAAGTTTCT TTCCTAAACC ATTCACCAAG AGCCAATATC 6780 TAGGCATTTT CTTGGTAGCA CAAATTTTCT TATTGCTTAG AAAATTGTCC TCCTTGTTAT 6840 TTCTGTTTGT AAGACTTAAG TGAGTTAGGT CTTTAAGGAA AGCAACGCTC CTCTGAAATG 6900 CTTGTCTTTT TTCTGTTGCC GAAATAGCTG GTCCTTTTTC GGGAGTTAGA TGTATAGAGT 6960 GTTTGTATGT AAACATTTCT TGTAGGCATC ACCATGAACA AAGATATATT TTCTATTTAT 7020 TTATTATATG TGCACTTCAA GAAGTCACTG TCAGAGAAAT AAAGAATTGT CTTAAATGTC Seq ID NO: 16 Protein sequence: Protein Accession #: XP_051860.2 1   11   21   31   41   51 |  |   |    |   |   | MGAAGRQDFL FKAMLTISWL TLTCFPGATS TVAAGCPDQS PELQPWNPGH DQDHHVHIGQ 60 GKTLLLTSSA TVYSIHISEG GKLVIKDHDE PIVLRTRHIL IDNGGELHAG SALCPFQGNF 120 TIILYGRADE GIQPDPYYGL KYIGVGKGGA LELHGQKKLS WTFLNKTLHP GGMAEGGYFF 180 ERSWGHRGVI VHVIDPKSGT VIHSDRFDTY RSKKESERLV QYLNAVPDGR ILSVAVNDEG 240 SRNLDDMARK AMTKLGSKHF LHLGFRHPWS FLTVKGNPSS SVEDHIEYHG HRGSAAARVF 300 KLFQTEHGEY FNVSLSSEWV QDVEWTEWFD HDKVSQTKGG EKISDLWKAH PGKICNRPID 360 IQATTMDGVN LSTEVVYKKG QDYRFACYDR GRACRSYRVR FLCGKPVRPK LTVTIDTNVN 420 STILNLEDNV QSWKPGDTLV IASTDYSMYQ AEEFQVLPCR SCAPNQVKVA GKPMYLHIGE 480 EIDGVDMRAE VGLLSRNIIV MGEMEDKCYP YRNHICNFFD FDTFGGHIKF ALGFKAAHLE 540 GTELKHMGQQ LVGQYPIHFH LAGDVDERGG YDPPTYIRDL SIHHTFSRCV TVHGSNGLLI 600 KDVVGYNSLG HCFFTEDGPE ERNTFDHCLG LLVKSGTLLP SDRDSKMCKM ITEDSYPGYI 660 PKPRQDCNAV STFWMANPNN NLINCAAAGS EETGFWFIFH HVPTGPSVGM YSPGYSEHIP 720 LGKFYNNRAH SNYRAGMIID NGVKTTEASA KDKRPFLSII SARYSPHQDA DPLKPREPAI 780 IRHFIAYKNQ DHGAWLRGGD VWLDSCRFAD NGIGLTLASG GTFPYDDGSK QEIKNSLFVG 840 ESGNVGTEMM DNRIWGPGGL DHSGRTLPIG QNFPIRGIQL YDGPINIQNC TFRKFVALEG 900 RHTSALAFRL NNAWQSCPHN NVTGIAFEDV PITSRVFFGE PGPWFNQLDM DGDKTSVFHD 960 VDGSVSEYPG SYLTKNDNWL VRHPDCINVP DWRGAICSGC YAQMYIQAYK TSNLRMKIIK 1020 NDFPSHPLYL EGALTRSTHY QQYQPVVTLQ KGYTIHWDQT APAELAIWLI NFNKGDWIRV 1080 GLCYPRGTTF SILSDVHNRL LKQTSKTGVF VRTLQMDKVE QSYPGRSHYY WDEDSGLLFL 1140 KLKAQNEREK FAFCSMKGCE RIKIKALIPK NAGVSDCTAT AYPKFTERAV VDVPMPKKLF 1200 GSQLKTKDHF LEVKMESSKQ HFFHLWNDFA YIEVDGKKYP SSEDGIQVVV IDGNQGRVVS 1260 HTSFRNSILQ GIPWQLFNYV ATIPDNSIVL MASKGRYVSR GPWTRVLEKL GADRGLKLKE 1320 QMAFVGFKGS FRPIWVTLDT EDHKAKIFQV VPIPVVKKKK L Seq ID NO: 17 DNA sequence Nucleic Acid Accession #: NM_015515.1 Coding sequence: 61-1329 1   11   21   31   41   51 |  |   |    |   |   | AGTTCTGCGG TGCCAGGGAG TGGAGCAGAG CTCAGCCCCG TCCCAAACAC AGATGGGACC 60 ATGAACTCCG GACACAGCTT CAGCCAGACC CCCTCGGCCT CCTTCCATGG CGCCGGAGGT 120 GGCTGGGGCC GGCCCAGGAG CTTCCCCAGG GCTCCCACCG TCCATGGCGG TGCGGGGGGA 180 GCCCGCATCT CCCTGTCCTT CACCACGCGG AGCTGCCCAC CCCCTGGAGG GTCTTGGGGT 240 TCTGGAAGAA GCAGCCCCCT ACTAGGCGGA AATGGGAAGG CCACCATGCA GAATCTCAAC 300 GACCGCCTGG CCTCCTACCT GGAGAAGGTT CGCGCCCTGG AGGAGGCCAA CATGAAGCTG 360 GAAAGCCGCA TCCTGAAATG GCACCAGGAG AGAGATCCTG GCAGTAAGAA AGATTATTCC 420 CAGTATGAGG AAAACATCAC ACACCTGCAG GAGCAGATAG TGGATGGTAA GATGACCAAT 480 GCTCAGATTA TTCTTCTCAT TGACAATGCC AGGATGGCAG TGGATGACTT CAACCTCAAG 540 TATGAAAATG AACACTCCTT TAAGAAAGAC TTGGAAATTG AAGTCGAGGG CCTCCGAAGG 600 ACCTTAGACA ACCTGACCAT TGTCACAACA GACCTAGAAC AGGAGGTGGA AGGAATGAGG 660 AAAGAGCTCA TTCTCATGAA GGAGCACCAT GAGCAGGAAA TGGAGGAGCA TCATGTGCCA 720 AGTGACTTCA ATGTCAATGT GAAGGTGGAT ACAGGTCCCA GGGAAGATCT GATTAAGGTC 780 CTGGAGGATA TGAGACAAGA ATATGAGCTT ATAATAAAGA AGAAGCATCG AGACTTGGAC 840 ACTTGGTATA AAGAACAGTC TGCAGCCATG TCCCAGGAGG CAGCCAGTCC AGCCACTGTG 900 CAGAGCAGAC AAGGTGACAT CCACGAACTG AAGCGCACAT TCCAGGCCCT GGAGATTGAC 960 CTGCAGGCAC AGTACAGCAC GAAATCTGCT TTGGAAAACA TGTTATCCGA GACCCAGTCT 1020 CGGTACTCCT GCAAGCTCCA GGACATGCAA GAGATCATCT CCCACTATGA GGAGGAACTG 1080 ACGCAGCTAC GCCACGAACT GGAGCGGCAG AACAATGAAT ACCAAGTGCT GCTGGGCATC 1140 AAAACCCACC TGGAGAAGGA AATCACCACG TACCGACGGC TCCTGGAGGG AGAGAGTGAA 1200 GGGACACGGG AAGAATCAAA GTCGAGCATG AAAGTGTCTG CAACTCCAAA GATCAAGGCC 1260 ATAACCCAGG AGACCATCAA CGGAAGATTA GTTCTTTGTC AAGTGAATGA AATCCAAAAG 1320 CACGCATGAG ACCAATGAAA GTTTCCGCCT GTTGTAAAGT CTATTTTCCC CCAAGGAAAG 1380 TCCTTGCACA GACACCAGTG AGTGAGTTCT AAAAGATACC CTTGGAATTA TCAGACTCAG 1440 AAACTTTTAT TTTTTTTTTT CTGTAACAGT CTCACCAGAC TTCTCATAAT GCTCTTAATA 1500 TATTGCACTT TTCTAATCAA AGTGCGAGTT TATGAGGGTA AAGCTCTACT TTCCTACTGC 1560 AGCCTTCAGA TTCTCATCAT TTTGCATCTA TTTTGTAGCC AATAAAACTC CGCACTAGC Seq ID NO: 18 Protein sequence: Protein Accession #: NP_056330.1 1   11   21   31   41   51 |  |   |    |   |   | MNSGHSFSQT PSASFHGAGG GWGRPRSFPR APTVHGGAGG ARISLSFTTR SCPPPGGSWG 60 SGRSSPLLGG NGKATMQNLN DRLASYLEKV RALEEANMKL ESRILKWHQQ RDPGSKKDYS 120 QYEENITHLQ EQIVDGKMTN AQIILLIDNA RMAVDDFNLK YENEHSFKKD LEIEVEGLRR 180 TLDNLTIVTT DLEQEVEGMR KELILMKEHH EQEMEEHHVP SDFNVNVKVD TGPREDLIKV 240 LEDMRQEYEL IIKKKHRDLD TWYKEQSAAM SQEAASPATV QSRQGDIHEL KRTFQALEID 300 LQAQYSTKSA LENMLSETQS RYSCKLQDMQ EIISHYEEEL TQLRHELERQ NNEYQVLLGI 360 KTHLEKEITT YRRLLEGESE GTREESKSSM KVSATPKIKA ITQETINGRL VLCQVNEIQK 420 HA Seq ID NO: 19 DNA sequence Nucleic Acid Accession #: see Table 25 & 25A for complete list 1   11   21   31   41   51 |  |   |    |   |   | TTTTTTTTTT TTAAAAAAAA GAGGCTTGGT AAGTTTTTGA TACTTAGTTG ACTTTTAGCA 60 TTATCCAGCA TTFGTATTAT GAACCAGTGA GTACTGTAAT TTTTCTTTCC CTTTCAGAAA 120 GACTCAAAGG GAACATATAA ATGTTTCCTA TTTTTNNNNN NNNNNNNNNN NNNNNNNNNN 180 NNNNACCCAT CGTGCGATGA TCNNNNNNNN NNNNNNNNNN NNNNNTTGGG ATCCAGTTTC 240 AAATAAGGTA TGGGAAAAAC AGATGTTTTC ATTATCGCCA CTTAATCCTT ACTTCCGATT 300 ATAATTATAC ATGTTTGGCT GTAATAACTA TACTAAAGCA TGCTTGTGAA AGTAGACTTC 360 TACAAGGACA GAAAACCCAC AACAACAAAG ATCGATCACG AAAGACAAGG CATATTCATT 420 CATTAATTTA CTTCTCTTAG ACCCGGGACA TGTGGGACAA ATACTTTTGT CCTCATGGAT 480 GGCTTGATAA TTTATTTATA TGTTCTAGAG TCTGAGGATT TTCTTTCAGT GGCAGACAAC 540 AAAGGATGTT ACAATTTACT TCAAAATAAT ACAATCATGG TTTAATTTAC AGTGTAAATC 600 CATAACTATT TTATAGAGAT GGATTATCAT ACATGGGATT ATAAAAATAA CTTACCCATA 660 TGCTTGCAAA ATAGACTTTT CCTATTGGGA GGAACATCTT TTAACCTAAA ACGGATTTAT 720 TTCAGATGAA TTAGACAGTA CATTTTTCAG GAGAACCAGC CTTACTGGAT GATCTTTTGT 780 CAGGTTTGGA GGCCTCTTCT TTGTCTTTGC AACCATAACC CCTTTTCAGC TGAAGACCAC 840 TGGCCTTCAA CCCAAGCCAG GAGTTTGGCT CAAATGA Seq ID NO: 20 DNA sequence Nucleic Acid Accession #: D3205 1.1 Coding sequence: 72-1373 1   11   21   31   41   51 |  |   |    |   |   | GAATTCGAAC CAGGTGGCCA CCCGGTGTCG GTTTCATTTT CCTTTGGAAT TTCTGCTTTA 60 CAGACAGAAC AATGGCAGCC CGAGTACTTA TAATTGGCAG TGGAGGAAGG GAACATACGC 120 TGGCCTGGAA ACTTGCACAG TCTCATCATG TCAAACAAGT GTTGGTTGCC CCAGGAAACG 180 CAGGCACTGC CTGCTCTGAA AAGATTTCAA ATACCGCCAT CTCAATCAGT GACCACACTG 240 CCCTTGCTCA ATTCTGCAAA GAGAAGAAAA TTGAATTTGT AGTTGTTGGA CCAGAAGCAC 300 CTCTGGCTGC TGGGATTGTT GGGAACCTGA GGTCTGCAGG AGTGCAATGC TTTGGCCCAA 360 CAGCAGAAGC GGCTCAGTTA GAGTCCAGCA AAAGGTTTGC CAAAGAGTTT ATGGACAGAC 420 ATGGAATCCC AACCGCACAA TGGAAGGCTT TCACCAAACC TGAAGAAGCC TGCAGCTTCA 480 TTTTGAGTGC AGACTTCCCT GCTTTGGTTG TGAAGGCCAG TGGTCTTGCA GCTGGAAAAG 540 GGGTGATTGT TGCAAAGAGC AAAGAAGAGG CCTGCAAAGC TGTACAAGAG ATCATGCAGG 600 AGAAAGCCTT TGGGGCAGCT GGAGAAACAA TTGTCATTGA AGAACTTCTT GACGGAGAAG 660 AGGTGTCGTG TCTGTGTTTC ACTGATGGCA AGACTGTGGC CCCCATGCCC CCAGCACAGG 720 ACCATAAGCG ATTACTGGAG GGAGATGGTG GCCCTAACAC AGGGGGAATG GGAGCCTATT 780 GTCCAGCCCC TCAGGTTTCT AATGATCTAT TACTAAAAAT TAAAGATACT GTTCTTCAGA 840 GGACAGTGGA TGGCATGCAG CAAGAGGGTA CTCCATATAC AGGTATTCTC TATGCTGGAA 900 TAATGCTGAC CAAGAATGGC CCAAAAGTTC TAGAGTTTAA TFGCCGTTTT GGTGATCCAG 960 AGTGCCAAGT AATCCTCCCA CTTCTTAAAA GTGATCTTTA TGAAGTGATT CAGTCCACCT 1020 TAGATGGACT GCTCTGCACA TCTCTGCCTG TTTGGCTAGA AAACCACACC GCCCTAACTG 1080 TTGTCATGGC AAGTAAAGGT TATCCTGGAG ACTACACCAA GGGTGTAGAG ATAACAGGGT 1140 TTCCTGAGGC TCAAGCTCTA GGACTGGAGG TGTCCCATGC AGGCACTGCC CTCAAAAATG 1200 GCAAAGTAGT AACTCATGGG GGTAGAGTTC TTGCAGTCAC AGCCATCCGG GAAAATCTCA 1260 TATCAGCCCT TGAGGAAGCC AAGAAAGGAC TAGCTGCTAT AAAGTTTGAG GGAGCAATTT 1320 ATAGGAAAGA CATCGGCTTT CGTGCCATAG CTTTCCTCCA GCAGCCCAGG TAAAACTCTA 1380 AGCAAGTTAG CTGTAGTGCC ATTTCAGAAA CTGGCCTAAA TGGCTATGTA GAACATTCCA 1440 TTAACCCTAT AAGTCATTCA GTATTCTTTT CTCTCTGTGG GAGTGATACA GTCTTGGTTT 1500 GTATTTTGTT TGAATCAAAA CTGGTTATAG CAATACTCAA ATGGAAAAAA CTTCATGATA 1560 GCGTAAGTTT GGAAAGTTTA GCAAAATCAC AGTGGTACTG ATTTTTATTT GTTTTCTATT 1620 TTTTTTATTT TATATTTTTA ATTTTTTTAA CAGGGTCTTC CTCTCTCGCC CAAGTTCTCA 1680 TGCCTCAGCC TCCCAAATAG CTGGGACTAC AGGCACAGGC CACCACACCT GGCTAATTTT 1740 TTTGTATTTT TTGTGGAGAT GGGGTTCACC ATGTTGCCAA GGCCAGTCTG AAAGCCTGGG 1800 CTCAAGTGAT CCTCCTGCTT TGGCCTCCCA AAATGCTGGG ACTATAGGCA TGAGGCGCTG 1860 CACTTGGCCT GATACTGATT TTTATTCCTT GCGTTATCAC ATAGTGTTGT ATTTGAAACA 1920 TAGTTCATGG TTTTATCAAA GAACTGAAGA TGAGAATACT GGTCATCTAA CTTTGTAATT 1980 TGATTTGATT ATACTGTAAA GTTTGACAGT CCCATTTTAA CCTGCGTTTG TATCTATTAC 2040 TAAAATGTAT TTTTTGACCT CTTACTGATT CATGGTTGGT ATGTACAAAC TGTTGACTTG 2100 TAAAATCAAT AAAGTCTTAG TTGG Seq ID NO: 21 Protein sequence: Protein Accession #: BA.A06809.1 1   11   21   31   41   51 |  |   |    |   |   | MAARVLIIGS GGREHTLAWK LAQSHHVKQV LVAPGNAGTA CSEKISNTAI SISDHTALAQ 60 FCKEKKIEFV VVGPEAPLAA GIVGNLRSAG VQCFGPTAEA AQLESSKRFA KEFMDRHGIP 120 TAQWKAFTKP EEACSFILSA DFPALVVKAS GLAAGKGVIV AKSKEEACKA VQEIMQEKAF 180 GAAGETIVIE ELLDGEEVSC LCFTDGKTVA PMPPAQDHKR LLEGDGGPNT GGMGAYCPAP 240 QVSNDLLLKI KDTVLQRTVD GMQQEGTPYT GILYAGIMLT KNGPKVLEFN CRFGDPECQV 300 ILPLLKSDLY EVIQSTLDGL LCTSLPVWLE NHTALTVVMA SKGYPGDYTK GVEITGFPEA 360 QALGLEVSHA GTALKNGKVV THGGRVLAVT AIRENLISAL EEAKKGLAAI KFEGAIYRKD 420 IGFRAIAFLQ QPR Seq ID NO: 22 DNA sequence Nucleic Acid Accession #: EOS cloned Coding sequence: 1-2424 1   11   21   31   41   51 |  |   |    |   |   | ATGCCCCCTT TCCTGTTGCT GGAGGCCGTC TGTGTTTTCC TGTTTTCCAG AGTGCCCCCA 60 TCTCTCCCTC TCCAGGAAGT CCATGTAAGC AAAGAAACCA TCGGGAAGAT TTCAGCTGCC 120 AGCAAAATGA TGTGGTGCTC GGCTGCAGTG GACATCATGT TTCTGTTAGA TGGGTCTAAC 180 AGCGTCGGGA AAGGGAGCTT TGAAAGGTCC AAGCACTTTG CCATCACAGT CTGTGACGGT 240 CTGGACATCA GCCCCGAGAG GGTCAGAGTG GGAGCATTCC AGTTCAGTTC CACTCCTCAT 300 CTGGAATTCC CCTTGGATTC ATTTTCAACC CAACAGGAAG TGAAGGCAAG AATCAAGAGG 360 ATGGTTTTCA AAGGAGGGCG CACGGAGACG GAACTTGCTC TGAAATACCT TCTGCACAGA 420 GGGTTGCCTG GAGGCAGAAA TGCTTCTGTG CCCCAGATCC TCATCATCGT CACTGATGGG 480 AAGTCCCAGG GGGATGTGGC ACTGCCATCC AAGCAGCTGA AGGAAAGGGG TGTCACTGTG 540 TTTGCTGTGG GGGTCAGGTT TCCCAGGTGG GAGGAGCTGC ATGCACTGGC CAGCGAGCCT 600 AGAGGGCAGC ACGTGCTGTT GGCTGAGCAG GTGGAGGATG CCACCAACGG CCTCTTCAGC 660 ACCCTCAGCA GCTCGGCCAT CTGCTCCAGC GCCACGCCAG ACTGCAGGGT CGAGGCTCAC 720 CCCTGTGAGC ACAGGACGCT GGAGATGGTC CGGGAGTTCG CTGGCAATGC CCCATGCTGG 780 AGAGGATCGC GGCGGACCCT TGCGGTGCTG GCTGCACACT GTCCCTTCTA CAGCTGGAAG 840 AGAGTGTTCC TAACCCACCC TGCCACCTGC TACAGGACCA CCTGCCCAGG CCCCTGTGAC 900 TCGCAGCCCT GCCAGAATGG AGGCACATGT GTTCCAGAAG GACTGGACGG CTACCAGTGC 960 CTCTGCCCGC TGGCCTTTGG AGGGGAGGCT AACTGTGCCC TGAAGCTGAG CCTGGAATGC 1020 AGGGTCGACC TCCTCTTCCT GCTGGACAGC TCTGCGGGCA CCACTCTGGA CGGCTTCCTG 1080 CGGGCCAAAG TCTTCGTGAA GCGGTTTGTG CGGGCCGTGC TGAGCGAGGA CTCTCGGGCC 1140 CGAGTGGGTG TGGCCACATA CAGCAGGGAG CTGCTGGTGG CGGTGCCTGT GGGGGAGTAC 1200 CAGGATGTGC CTGACCTGGT CTGGAGCCTC GATGGCATTC CCTTCCGTGG TGGCCCCACC 1260 CTGACGGGCA GTGCCTTGCG GCAGGCGGCA GAGCGTGGCT TCGGGAGCGC CACCAGGACA 1320 GGCCAGGACC GGCCACGTAG AGTGGTGGTT TTGCTCACTG AGTCACACTC CGAGGATGAG 1380 GTTGCGGGCC CAGCGCGTCA CGCAAGGGCG CGAGAGCTGC TCCTGCTGGG TGTAGGCAGT 1440 GAGGCCGTGC GGGCAGAGCT GGAGGAGATC ACAGGCAGCC CAAAGCATGT GATGGTCTAC 1500 TCGGATCCTC AGGATCTGTT CAACCAAATC CCTGAGCTGC AGGGGAAGCT GTGCAGCCGG 1560 CAGCGGCCAG GGTGCCGGAC ACAAGCCCTG GACCTCGTCT TCATGTTGGA CACCTCTGCC 1620 TCAGTAGGGC CCGAGAATTT TGCTCAGATG CAGAGCTTTG TGAGAAGCTG TGCCCTCCAG 1680 TTTGAGGTGA ACCCTGACGT GACACAGGTC GGCCTGGTGG TGTATGGCAG CCAGGTGCAG 1740 ACTGCCTTCG GGCTGGACAC CAAACCCACC CGGGCTGCGA TGCTGCGGGC CATTAGCCAG 1800 GCCCCCTACC TAGGTGGGGT GGGCTCAGCC GGCACCGCCC TGCTGCACAT CTATGACAAA 1860 GTGATGACCG TCCAGAGGGG TGCCCGGCCT GGTGTCCCCA AAGCTGTGGT GGTGCTCACA 1920 GGCGGGAGAG GCGCAGAGGA TGCAGCCGTT CCTGCCCAGA AGCTGAGGAA CAATGGCATC 1980 TCTGTCTTGG TCGTGGGCGT GGGGCCTGTC CTAAGTGAGG GTCTGCGGAG GCTTGCAGGT 2040 CCCCGGGATT CCCTGATCCA CGTGGCAGCT TACGCCGACC TGCGGTACCA CCAGGACGTG 2100 CTCATTGAGT GGCTGTGTGG AGAAGCCAAG CAGCCAGTCA ACCTCTGCAA ACCCAGCCCG 2160 TGCATGAATG AGGGCAGCTG CGTCCTGCAG AATGGGAGCT ACCGCTGCAA GTGTCGGGAT 2220 GGCTGGGAGG GCCCCCACTG CGAGAACCGT GAGTGGAGCT CTTGCTCTGT ATGTGTGAGC 2280 CAGGGATGGA TTCTTGAGAC GCCCCTGAGG CACATGGCTC CCGTGCAGGA GGGCAGCAGC 2340 CGTACCCCTC CCAGCAACTA CAGAGAAGGC CTGGGCACTG AAATGGTGCC TACCTTCTGG 2400 AATGTCTGTG CCCCAGGTCC TTAG Seq ID NO: 23 Protein sequence: Protein Accession #: EOS cloned 1   11   21   31   41   51 |  |   |    |   |   | MPPFLLLEAV CVFLFSRVPP SLPLQEVHVS KETIGKISAA SKMMWCSAAV DIMFLLDGSN 60 SVGKGSFERS KHFAITVCDG LDISPERVRV GAFQFSSTPH LEFPLDSFST QQEVKARIKR 120 MVFKGGRTET ELALKYLLHR GLPGGRNASV PQILIIVTDG KSQGDVALPS KQLKERGVTV 180 FAVGVRFPRW EELHALASEP RGQHVLLAEQ VEDATNGLFS TLSSSAICSS ATPDCRVEAH 240 PCEHRTLEMV REFAGNAPCW RGSRRTLAVL AAHCPFYSWK RVFLTHPATC YRTTCPGPCD 300 SQPCQNGGTC VPEGLDGYQC LCPLAFGGEA NCALKLSLEC RVDLLFLLDS SAGTTLDGFL 360 RAKVFVKRFV RAVLSEDSRA RVGVATYSRE LLVAVPVGEY QDVPDLVWSL DGIPFRGGPT 420 LTGSALRQAA ERGFGSATRT GQDRPRRVVV LLTESHSEDE VAGPARHARA RELLLLGVGS 480 EAVRAELEEI TGSPKHVMVY SDPQDLFNQI PELQGKLCSR QRPGCRTQAL DLVFMLDTSA 540 SVGPENFAQM QSFVRSCALQ FEVNPDVTQV GLVVYGSQVQ TAFGLDTKPT RAAMLRAISQ 600 APYLGGVGSA GTALLHIYDK VMTVQRGARP GVPKAVVVLT GGRGAEDAAV PAQKLRNNGI 660 SVLVVGVGPV LSEGLRRLAG PRDSLIHVAA YADLRYHQDV LIEWLCGEAK QPVNLCKPSP 720 CMNEGSCVLQ NGSYRCKCRD GWEGPHCENR EWSSCSVCVS QGWILETPLR HMAPVQEGSS 780 RTPPSNYREG LGTEMVPTFW NVCAPGP Seq ID NO: 24 DNA sequence Nucleic Acid Accession #: see Table 25 & 25A for complete list 1   11   21   31   41   51 |  |   |    |   |   | AGGTCGGCTG GTTATCGGGA GTTGGAGGGC TGAGGTCGGG AGGGTGGTGT GTACAGAGCT 60 CTAGGACTCA CGCACCAGGC CAGTCGCGGG TTTTGGGCCG AGGCCTGGGT TACAAGCAGC 120 AAGTGCGCGG TTGGGGCCAC TGCGAGGCCG TTTTAGAAAA CTGTTTAAAA CAAAGAGCAA 180 TTGATGGATA AATCAGGAAT AGATTCTCTT GACCATGTGA CATCTGATGC TGTGGAACTT 240 GCAAATCGAA GTGATAACTC TTCTGATAGC AGCTTATTTA AAACTCAGTG TATCCCTTAC 300 TCACCTAAAG GGGAGAAAAG AAACCCCATT CGAAAATTTG TTCGTACACC TGAAAGTGTT 360 CACGCAAGTA TTCATCAAGT GACTCATCTT TTGAACCAGT ACCATTGACT ATAAAAGCTA 420 TTTTTGAAAG ATTCAAGAAC AGGAAAAAGA GATATAAAAA AAAGAAAAAG AGGAGGTACC 480 AGCCAACAGG AAGACCACGG GGAAGACCAG AAGGAAGGAG AAATCCTATA TACTCACTAA 540 TAGATAAGAA GAAACAATTT AGAAGCAGAG GATCTGGCTT CCCATTTTTA GAATCAGAGA 600 ATGAAAAAAA CGCACCTTGG AGAAAAATTT TAACGTTTGA GCAAGCTGTT GCAAGAGGAT 660 TTTTTAACTA TATTGAAAAA CTGAAGTATG AACACCACCT GAAAGAATCA TTGAAGCAAA 720 TGAATGTTGG TGAAGATTTA GAAAATGAAG ATTTTGACAG TCGTAGATAC AAATTTTTGG 780 ATGATGATGG ATCCATTTCT CCTATTGAGG AGTCAACGCT TTTATCTTGA GGACATGGTG 840 TCTGGAGTTA AAGGTATTGG CATACTCCAC ACATCTGTAC CATTCTTGAG TGATCGCTTA 900 GGAATGAATG TGATTTGGAC TCATTCATGT ATGAGAGTAA GCAATGCTTT TTTTTCCAGG 960 GTGTCAAATT GAGAACCAGG TAGATCCCCA CCACCTACAG TAAAAAGGAC CCTAAAGTAA 1020 ATTGGTTGAA GAAATTAGAT CCCAAAGATT CTTGGTGAAT TTTGAAGTCT TCATCAGTAT 1080 ATCCATATTA AAACGAGATG ACAGAAGCCA AAGTAATTAT GGGCTGACAG GACAACTGGA 1140 TCAGTTTCAT TAAAAAGGGC AAACTTGAAG ATAAATCTTT TGACTCCAGC TCTTTAGAGG 1200 ATCTAAAGTG ACCTTGATGG ACAGTGGAAG AAATCACAAC ATGGAATTCC TCGAATAACA 1260 ATTTATTGAC TTTAAATAAT TTTGTCTAAT GCTACATATA CACAATTAAA AAACCTTTAC 1320 ACTATTTCTA GAAAGTCAGC ATGTATTTTT GGCTCGAAGT TTCTCTAGTT TTTTCTGTGG 1380 AAGGAATAAA AATTTGAGGT TTCAATACAA AAACAAAACA AACAACACGA AACACGAAAA 1440 ACAATCTGTT GTGCGGCGCC CCTGGGCCCC TTGAGAGAAA ACTTTTTAGA ACCCCTTTTG 1500 CGTTGTGGCG GCCCGGGGGC CCCACAGTTG GGTTTAGGTG GGCACCCTTG TGTCTACAAG 1560 TGGTGTCTCC CCAAGAGAGA GAACACCTCC GGGGTCAAGC GGACAACAAG AGTGCGTCGT 1620 GAGGACTCTT CACCCAAAGT ATATAAAACC CGCCCCGCGG GGGAACCACC GGCCGCTTTT 1680 CTGTAGACAC AACCCCCACA GTGGGAACCT CTGAGGGCGC ACACACAGGG CGAGCCTTAT 1740 CAACAAGGGG TGCCCAACAG AAACCCCGAG TTAAAAATCG Seq ID NO: 25 DNA sequence Nucleic Acid Accession #: BC001972.1 Coding sequence: 183-1019 1   11   21   31   41   51 |  |   |    |   |   | GGTCGGCTGG TTATCGGGAG TTGGAGGGCT GAGGTCGGGA GGGTGGTGTG TACAGAGCTC 60 TAGGACTCAC GCACCAGGCC AGTCGCGGGT TTTGGGCCGA GGCCTGGGTT ACAAGCAGCA 120 AGTGCGCGGT TGGGGCCACT GCGAGGCCGT TTTAGAAAAC TGTTTAAAAC AAAGAGCAAT 180 TGATGGATAA ATCAGGAATA GATTCTCTTG ACCATGTGAC ATCTGATGCT GTGGAACTTG 240 CAAATCGAAG TGATAACTCT TCTGATAGCA GCTTATTTAA AACTCAGTGT ATCCCTTACT 300 CACCTAAAGG GGAGAAAAGA AACCCCATTC GAAAATTTGT TCGTACACCT GAAAGTGTTC 360 ACGCAAGTGA TTCATCAAGT GACTCATCTT TTGAACCAAT ACCATTGACT ATAAAAGCTA 420 TTTTTGAAAG ATTCAAGAAC AGGAAAAAGA GATATAAAAA AAAGAAAAAG AGGAGGTACC 480 AGCCAACAGG AAGACCACGG GGAAGACCAG AAGGAAGGAG AAATCCTATA TACTCACTAA 540 TAGATAAGAA GAAACAATTT AGAAGCAGAG GATCTGGCTT CCCATTTTTA GAATCAGAGA 600 ATGAAAAAAA CGCACCTTGG AGAAAAATTT TAACGTTTGA GCAAGCTGTT GCAAGAGGAT 660 TTTTTAACTA TATTGAAAAA CTGAAGTATG AACACCACCT GAAAGAATCA TTGAAGCAAA 720 TGAATGTTGG TGAAGATTTA GAAAATGAAG ATTTTGACAG TCGTAGATAC AAATTTTTGG 780 ATGATGATGG ATCCATTTCT CCTATTGAGG AGTCAACAGC AGAGGATGAG GATGCAACAC 840 ATCTTGAAGA TAACGAATGT GATATCAAAT TGGCAGGGGA TAGTTTCATA GTAAGTTCTG 900 AATTCCCTGT AAGACTGAGT GTATACTTAG AAGAAGAGGA TATTACTGAA GAAGCTGCTT 960 TGTCTAAAAA GAGAGCTACA AAAGCCAAAA ATACTGGACA GAGAGGCCTG AAAATGTGAC 1020 AGGATCATGA ATGTCAAAGG CTTTTATCTT GAGAACATGG TGTCTGGAGT TAAAGGACTA 1080 TTGTTAGATC TGTGGGAAGG AATTACAAGA CAGTTGCTAA AAGTTTGAAA AAGACGGTTG 1140 CTAAACGTTA TGAAAAACCA GATAATCTAC TTTTTTACCT TAGGTATTGG CATACTCCAC 1200 ACATCTGTAC CATTCTTGAG TGATCGCTTA GGAATGAATG TGATTTGAAC TCATTCATGT 1260 TGAGAGGGTG TCAAATTGAG AACCAGGTAG ATCCCCACCA CCTACAGTAA AAAGGACCCT 1320 AAAGTAAATT GGTTGAAGAA ATTAGATCCC AAAGATTCTT GGTGAATTTT GAAGTCTTCA 1380 TCAGTATATC CATATTAAAA CGAGATGACA GAAGCCAAAG TAATTATGGG CTGACAGGAC 1440 AACTGGATCA GTTTCATTAA AAAGGGCAAA CTTGAAGATA AATCTTTTGA CTCCAGCTCT 1500 TTAGAGGATC TAAAGTGACC TTGATGGACA GTGGAAGAAA TCACAACATG GAATTCCTCG 1560 AATAACAATT TATTGACTTT AAATAATTTT GTCTAATGCT ACATATACAC AATTAAAAAA 1620 CCTTTACACT AAAAAAAAAA AAAAAA Seq ID NO: 26 Protein sequence: Protein Accession #: AAH01972.1 1   11   21   31   41   51 |  |   |    |   |   | MDKSGIDSLD HVTSDAVELA NRSDNSSDSS LFKTQCIPYS PKGEKRNPIR KFVRTPESVH 60 ASDSSSDSSF EPIPLTIKAI FERFKNRKKR YKKKKKRRYQ PTGRPRGRPE GRRNPIYSLI 120 DKKKQFRSRG SGFPFLESEN EKNAPWRKIL TFEQAVARGF FNYIEKLKYE HHLKESLKQM 180 NVGEDLENED FDSRRYKFLD DDGSISPIEE STAEDEDATH LEDNECDIKL AGDSFIVSSE 240 FPVRLSVYLE EEDITEEAAL SKKRATKAKN TGQRGLKM Seq ID NO: 27 DNA sequence Nucleic Acid Accession #: AK027016 Coding sequence: 207-1043 1   11   21   31   41   51 |  |   |    |   |   | CTTTTCTTCC GCACGGTTGG AGGAGGTCGG CTGGTTATCG GGAGTTGGAG GGCTGAGGTC 60 GGGAGGGTGG TGTGTACAGA GCTCTAGGAC TCACGCACCA GGCCAGTCGC GGATTTTGGG 120 CCGAGGCCTG GGTTACAAGC AGCAAGTGCG CGGTTGGGGC CACTGCGAGG CCGTTTTAGA 180 AAACTGTTTA AAACAAAGAG CAATTGATGG ATAAATCAGG AATAGATTCT CTTGACCATG 240 TGACATCTGA TGCTGTGGAA CTTGCAAATC GAAGTGATAA CTCTTCTGAT AGCAGCTTAT 300 TTAAAACTCA GTGTATCCCT TACTCACCTA AAGGGGAGAA AAGAAACCCC ATTCGAAAAT 360 TTGTTCGTAC ACCTGAAAGT GTTCACGCAA GTGATTCATC AAGTGACTCA TCTTTTGAAC 420 CAATACCATT GACTATAAAA GCTATTTTTG AAAGATTCAA GAACAGGAAA AAGAGATATA 480 AAAAAAAGAA AAAGAGGAGG TACCAGCCAA CAGGAAGACC ACGGGGAAGA CCAGAAGGAA 540 GGAGAAATCC TATATACTCA CTAATAGATA AGAAGAAACA ATTTAGAAGC AGAGGATCTG 600 GCTTCCCATT TTTAGAATCA GAGAATGAAA AAAACGCACC TTGGAGAAAA ATTTTAACGT 660 TTGAGCAAGC TGTTGCAAGA GGATTTTTTA ACTATATTGA AAAGCTGAAG TATGAACACC 720 ACCTGAAAGA ATCATTGAAG CAAATGAATG TTGGTGAAGA TTTAGAAAAT GAAGATTTTG 780 ACAGTCGTAG ATACAAATTT TTGGATGATG ATGGATCCAT TTCTCCTATT GAGGAGTCAA 840 CAGCAGAGGA TGAGGATGCA ACACATCTTG AAGATAACGA ATGTGATATC AAATTGGCAG 900 GGGATAGTTT CATAGTAAGT TCTGAATTCC CTGTAAGACT GAGTGTATAC TTAGAAGAAG 960 AGGATATTAC TGAAGAAGCT GCTETGTCTA AAAAGAGAGC TACAAAAGCC AAAAATACTG 1020 GACAGAGAGG CCTGAAAATG TGACAGGATC ATGAATGTCA AAGGCTTTTA TCTTGAGAAC 1080 ATGGTGTCTG GAGTTAAAGG TATTGGCATA CTCCACACAT CTGTACCATT CTTGAGTGAT 1140 CGCTTAGGAA TGAATGTGAT TTGAACTCAT TCATGTTGAG AGGGTGTCAA ATTGAGAACC 1200 AGGTAGATCC CCACCACCTA CAGTAAAAAG GACCCTAAAG TAAATTGGTT GAAGAAATTA 1260 GATCCCAAAG ATTCTTGGTG AATTTTGAAG TCTTCATCAG TATATCCATA TTAAAACGAG 1320 ATGACAGAAG CCAAAGTAAT TATGGCAAGT AATGGTTTTT ATCTTAACTA TAAGTTATTT 1380 GCTCAAGGGT GTAATGGTCA TTACCAAGGC TTTTAGAATG CAGTTTCTCA TTTGCTGTGG 1440 ACATGACCAT AAAAAAAAAT TTCCCAGTAG GTTTTCTATC TGCTACGTTG CTAGCAATCA 1500 GCTTATTGGG AACAGTTGAT TAACTGTAAT AGAAATGCAA TACAAATAAA ATGTGAACCA 1560 CATGTGATTT TTCTTTAAAA TCAGTGAGAT TTGAAAATTC TCCTAGATCT CTTGAATCAT 1620 GCAAATTTGC TTTGCCTTTA TATTGTAACC CTTGTGGGTT GCTAATAACC AAGCAGTTTG 1680 TAGTAGAGTT AACTCAGGCT CGTTCTAGGG ACTCATTCAT GTTCACTCAC TGTACACTCA 1740 TCTCTGGAAA TGTAAAATTT ACTTTTATAC TATTGTTATG TAGGGCTGAC AGGACAACTG 1800 GATCAGTTTC ATTAAAAAGG TATGTATGCA TTAGAAAAGA CATTTGTATG GGTCATTTCA 1860 AAGAGGGCTT ATGAGGCTGT GAAACCCAGA GCTCTTAACG CTGTGACCAA AGATGGAAGT 1920 TCTCTATAGG AAGCCATAGC ACTCCTAATG TTTGGTGCTA TGTTTTCCTG AGGAGATATA 1980 AAACGTAATA ATCCATGATT GTTGCCATGT GAGAGTTTTA AAGGTTAATC AAAATTTCTC 2040 TTCTTCAGGG CAAACTTGAA GATAAATCTT TTGACTCCAG CTCTTTAGAG GATCTAAAGT 2100 GACCTTGATG GACAGTGGAA GAAATCACAA CATGGAATTC CTCGAATAAC AATTTATTGA 2160 CTTTAAATAA TTTTGTCTAA TGCTACATAT ACACAATTAA AAAACCTTTA CACTATTTCT 2220 AGAAAGTCAG CATGTATTTT TGGCTCGAAG TTTCTCTAGT GTTTTCTGTG GAAGGAATAA 2280 AAATTTGAGT TTCAAAAAAA AAAAAAAAAA AAAAAAAAAA AAAAAAAAAA AAAAAA Seq ID NO: 28 Protein sequence: Protein Accession #: BAB15628.1 1   11   21   31   41   51 |  |   |    |   |   | MDKSGIDSLD HVTSDAVELA NRSDNSSDSS LFKTQCIPYS PKGEKRNPIR KFVRTPESVH 60 ASDSSSDSSF EPIPLTIKAI FERFKNRKKR YKKKKKRRYQ PTGRPRGRPE GRRNPIYSLI 120 DKKKQFRSRG SGFPFLESEN EKNAPWRKIL TFEQAVARGF FNYIEKLKYE HHLKESLKQM 180 NVGEDLENED FDSRRYKFLD DDGSISPIEE STAEDEDATH LEDNECDIKL AGDSFIVSSE 240 FPVRLSVYLE EEDITEEAAL SKKRATKAKN TGQRGLKM Seq ID NO: 29 DNA sequence Nucleic Acid Accession #: NM_004289.3 Coding sequence: 493.1695 1   11   21   31   41   51 |  |   |    |   |   | GCCGCCGCCT CGTCCACCGG AGGAGCCGGC GCCAGCGTGG ACGGCGGCAG CCAGGCTGTG 60 CAGGGGGGCG GCGGGGACCC CCGAGCGGCT CGGAGTGGCC CCTTGGACGC CGGGGAAGAG 120 GAGAAGGCAC CCGCGGAACC GACGGCTCAG GTGCCGGACG CTGGCGGATG TGCGAGCGAG 180 GAGAATGGGG TACTAAGAGA AAAGCACGAA GCTGTGGATC ATAGTTCCCA GCATGAGGAA 240 AATGAAGAAA GGGTGTCAGC CCAGAAGGAG AACTCACTTC AGCAGAATGA TGATGATGAA 300 AACAAAATAG CAGAGAAACC TGACTGGGAG GCAGAAAAGA CCACTGAATC TAGAAATGAG 360 AGACATCTGA ATGGGACAGA TACTTCTTTC TCTCTGGAAG ACTTATTCCA GTTGCTTTCA 420 TCACAGCCTG AAAATTCACT GGAGGGCATC TCATTGGGAG ATATTCCTCT TCCAGGCAGT 480 ATCAGTGATG GCATGAATTC TTCAGCACAT TATCATGTAA ACTTCAGCCA GGCTATAAGT 540 CAGGATGTGA ATCTTCATGA GGCCATCTTG CTTTGTCCCA ACAATACATT TAGAAGAGAT 600 CCAACAGCAA GGACTTCACA GTCACAAGAA CCATTTCTGC AGTTAAATTC TCATACCACC 660 AATCCTGAGC AAACCCTTCC TGGAACTAAT TTGACAGGAT TTCTTTCACC GGTTGACAAT 720 CATATGAGGA ATCTAACAAG CCAAGACCTA CTGTATGACC TTGACATAAA TATATTTGAT 780 GAGATAAACT TAATGTCATT GGCCACAGAA GACAACTTTG ATCCAATCGA TGTTTCTCAG 840 CTTTTTGATG AACCAGATTC TGATTCTGGC CTTTCTTTAG ATTCAAGTCA CAATAATACC 900 TCTGTCATCA AGTCTAATTC CTCTCACTCT GTGTGTGATG AAGGTGCTAT AGGTTATTGC 960 ACTGACCATG AATCTAGTTC CCATCATGAC TTAGAAGGTG CTGTAGGTGG CTACTACCCA 1020 GAACCCAGTA AGCTTTGTCA CTTGGATCAA AGTGATTCTG ATTTCCATGG AGATCTTACA 1080 TTTCAACACG TATTTCATAA CCACACTTAC CACTTACAGC CAACTGCACC AGAATCTACT 1140 TCTGAACCTT TTCCGTGGCC TGGGAAGTCA CAGAAGATAA GGAGTAGATA CCTTGAAGAC 1200 ACAGATAGAA ACTTGAGCCG TGATGAACAG CGTGCTAAAG CTTTGCATAT CCCTTTTTCT 1260 GTAGATGAAA TTGTCGGCAT GCCTGTTGAT TCTTTCAATA GCATGTTAAG TAGATATTAT 1320 CTGACAGACC TACAAGTCTC ACTTATCCGT GACATCAGAC GAAGAGGGAA AAATAAAGTT 1380 GCTGCGCAGA ACTGTCGTAA ACGCAAATTG GACATAATTT TGAATTTAGA AGATGATGTA 1440 TGTAACTTGC AAGCAAAGAA GGAAACTCTT AAGAGAGAGC AAGCACAATG TAACAAAGCT 1500 ATTAACATAA TGAAACAGAA ACTGCATGAC CTTTATCATG ATATTTTTAG TAGATTAAGA 1560 GATGACCAAG GTAGGCCAGT CAATCCCAAC CACTATGCTC TCCAGTGTAC CCATGATGGA 1620 AGTATCTTGA TAGTACCCAA AGAACTGGTG GCCTCAGGCC ACAAAAAGGA AACCCAAAAG 1680 GGAAAGAGAA AGTGAGAAGA AACTGAAGAT GGACTCTATT ATGTGAAGTA GTAATGTTCA 1740 GAAACTGATT ATTTGGATCA GAAACCATTG AAACTGCTTC AAGAATTGTA TCTTTAAGTA 1800 CTGCTACTTG AATAACTCAG TTAACGCTGT TTTGAAGCTT ACATGGACAA ATGTTTAGGA 1860 CTTCAAGATC ACACTTGTGG GCAATCTGGG GGAGCCACAA CTTTTCATGA AGTGCATTGT 1920 ATACAAAATT CATAGTTATG TCCAAAGAAT AGGTTAACAT GAAAACCCAG TAAGACTTTC 1980 CATCTTGGCA GCCATCCTTT TTAAGAGTAA GTTGGTTACT TCAAAAAGAG CAAACACTGG 2040 GGATCAAATT ATTTTAAGAG GTATTTCAGT TTTAAATGCA AAATAGCCTT ATTTTCATTT 2100 AGTTTGTTAG CACTATAGTG AGCTTTTCAA ACACTATTTT AATCTTTATA TTTAACTTAT 2160 AAATTTTGCT TTCT Seq ID NO: 30 Protein sequence: Protein Accession #: NP_004280 1   11   21   31   41   51 |  |   |    |   |   | MNSSAHYHVN FSQAISQDVN LHEAILLCPN NTFRRDPTAR TSQSQEPFLQ LNSHTTNPEQ 60 TLPGTNLTGF LSPVDNHMRN LTSQDLLYDL DINIFDEINL MSLATEDNFD PIDVSQLFDE 120 PDSDSGLSLD SSHNNTSVIK SNSSHSVCDE GAIGYCTDHE SSSHHDLEGA VGGYYPEPSK 180 LCHLDQSDSD FHGDLTFQHV FHNHTYHLQP TAPESTSEPF PWPGKSQKIR SRYLEDTDRN 240 LSRDEQRAKA LHIPFSVDEI VGMPVDSFNS MLSRYYLTDL QVSLIRDIRR RGKNKVAAQN 300 CRKRKLDIIL NLEDDVCNLQ AKKETLKREQ AQCNKAINIM KQKLHDLYHD IFSRLRDDQG 360 RPVNPNHYAL QCTHDGSILI VPKELVASGH KKETQKGKRK Seq ID NO: 31 DNA sequence Nucleic Acid Accession #: NM_033260.1 Coding sequence: 1-1208 1   11   21   31   41   51 |  |   |    |   |   | ATGAAGTTGG AGGTGTTCGT CCCTCGCGCG GCCCACGGGG ACAAGCAGGG CAGTGACCTG 60 GAGGGCGCGG GCGGCAGCGA CGCGCCGTCC CCGCTGTCGG CGGCGGGAGA CGACTCCCTG 120 GGCTCAGATG GGGACTGCGC GGCCAAGCCG TCCGCGGGCG GCGGCGCCAG AGATACGCAG 180 GGCGACGGCG AACAGAGTGC GGGAGGCGGG CCGGGCGCGG AGGAGGCGAT CCCGGCAGCA 240 GCTGCTGCAG CGGTGGTGGC GGAGGGCGCG GAGGCCGGGG CGGCGGGGCC AGGCGCGGGC 300 GGCGCGGGGA GCGGCGAGGG TGCACGCAGC AAGCCATATA CGCGGCGGCC CAAGCCCCCC 360 TACTCGTACA TCGCGCTCAT CGCCATGGCC ATCCGCGACT CGGCGGGCGG GCGCTTGACG 420 CTGGCGGAGA TCAACGAGTA CCTCATGGGC AAGTTCCCCT TTTTCCGCGG CAGCTACACG 480 GGCTGGCGCA ACTCCGTGCG CCACAACCTT TCGCTCAACG ACTGCTTCGT CAAGGTGCTG 540 CGCGACCCCT CGCGGCCCTG GGGCAAGGAC AACTACTGGA TGCTCAACCC CAACAGCGAG 600 TACACCTTCG CCGACGGGGT CTTCCGCCGC CGCCGCAAGC GCCTCAGCCA CCGCGCGCCG 660 GTCCCCGCGC CCGGGCTGCG GCCCGAGGAG GCCCCGGGCC TCCCCGCCGC CCCGCCGCCC 720 GCGCCCGCCG CCCCGGCCTC GCCCCGCATG CGCTCGCCCG CCCGCCAGGA GGAGCGCGCC 780 AGCCCCGCGG GCAAGTTCTC CAGCTCCTTC GCCATCGACA GCATCCTGCG CAAGCCTTTC 840 CGCAGCCGTC GCCTCAGGGA CACGGCCCCC GGGACGACGC TTCAGTGGGG CGCCGCGCCC 900 TGCCCGCCGC TGCCCGCGTT CCCCGCGCTC CTCCCCGCGG CGCCCTGCAG GGCCCTGCTG 960 CCGCTCTGCG CGTACGGCGC GGGCGAGCCG GCGCGGCTGG GCGCGCGCGA GGCCGAGGTG 1020 CCACCGACCG CGCCGCCCCT CCTGCTTGCA CCTCTCCCGG CGGCGGCCCC CGCCAAGCCA 1080 CTCCGAGGCC CGGCGGCCGG CGGCGCGCAC CTGTACTGCC CCCTGCGGCT GCCCGCAGCC 1140 CTGCAGGCGG CCTTAGTCCG NCGTCCTGGC CCGCACCTGT CGTACCCGGT GGAGACGCTC 1200 CTAGCTTGA Seq ID NO: 32 Protein sequence: Protein Accession #: NP_150285.1 1   11   21   31   41   51 |  |   |    |   |   | MKLEVFVPRA AHGDKQGSDL EGAGGSDAPS PLSAAGDDSL GSDGDCAAKP SAGGGARDTQ 60 GDGEQSAGGG PGAEEAIPAA AAAAVVAEGA EAGAAGPGAG GAGSGEGARS KPYTRRPKPP 120 YSYIALIAMA IRDSAGGRLT LAEINEYLMG KFPFFRGSYT GWRNSVRHNL SLNDCFVKVL 180 RDPSRPWGKD NYWMLNPNSE YTFADGVFRR RRKRLSHRAP VPAPGLRPEE APGLPAAPPP 240 APAAPASPRM RSPARQEERA SPAGKFSSSF AIDSILRKPF RSRRLRDTAP GTTLQWGAAP 300 CPPLPAFPAL LPAAPCRALL PLCAYGAGEP ARLGAREAEV PPTAPPLLLA PLPAAAPAKP 360 LRGPAAGGAH LYCPLRLPAA LQAALVRRPG PHLSYPVETL LA Seq 0) NO: 33 DNA sequence Nucleic Acid Accession #: NM_012128.2 Coding sequence: 43-2796 1   11   21   31   41   51 |  |   |    |   |   | GAACAAACCA ACATTTGAGC CAGGAATAAC TAGAGAGGAA CAATGGGGTT ATTCAGAGGT 60 TTTGTTTTCC TCTTAGTTCT GTGCCTGCTG CACCAGTCAA ATACTTCCTT CATTAAGCTG 120 AATAATAATG GCTTTGAAGA TATTGTCATT GTTATAGATC CTAGTGTGCC AGAAGATGAA 180 AAAATAATTG AACAAATAGA GGATATGGTG ACTACAGCTT CTACGTACCT GTTTGAAGCC 240 ACAGAAAAAA GATTTTTTTT CAAAAATGTA TCTATATTAA TTCCTGAGAA TTGGAAGGAA 300 AATCCTCAGT ACAAAAGGCC AAAACATGAA AACCATAAAC ATGCTGATGT TATAGTTGCA 360 CCACCTACAC TCCCAGGTAG AGATGAACCA TACACCAAGC AGTTCACAGA ATGTGGAGAG 420 AAAGGCGAAT ACATTCACTT CACCCCTGAC CTTCTACTTG GAAAAAAACA AAATGAATAT 480 GGACCACCAG GCAAACTGTT TGTCCATGAG TGGGCTCACC TCCGGTGGGG AGTGTTTGAT 540 GAGTACAATG AAGATCAGCC TTTCTACCGT GCTAAGTCAA AAAAAATCGA AGCAACAAGG 600 TGTTCCGCAG GTATCTCTGG TAGAAATAGA GTTTATAAGT GTCAAGGAGG CAGCTGTCTT 660 AGTAGAGCAT GCAGAATTGA TTCTACAACA AAACTGTATG GAAAAGATTG TCAATTCTTT 720 CCTGATAAAG TACAAACAGA AAAAGCATCC ATAATGTTTA TGCAAAGTAT TGATTCTGTT 780 GTTGAATTTT GTAACGAAAA AACCCATAAT CAAGAAGCTC CAAGCCTACA AAACATAAAG 840 TGCAATTTTA GAAGTACATG GGAGGTGATT AGCAATTCTG AGGATTTTAA AAACACCATA 900 CCCATGGTGA CACCACCTCC TCCACCTGTC TTCTCATTGC TGAAGATCCG TCAAAGAATT 960 GTGTGCTTAG TTCTTGATAA GTCTGGAAGC ATGGGGGGTA AGGACCGCCT AAATCGAATG 1020 AATCAAGCAG CAAAACATTT CCTGCTGCAG ACTGTTGAAA ATGGATCCTG GGTGGGGATG 1080 GTTCACTTTG ATAGTACTGC CACTATTGTA AATAAGCTAA TCCAAATAAA AAGCAGTGAT 1140 GAAAGAAACA CACTCATGGC AGGATTACCT ACATATCCTC TGGGAGGAAC TTCCATCTGC 1200 TCTGGAATTA AATATGCATT TCAGGTGATT GGAGAGCTAC ATTCCCAACT CGATGGATCC 1260 GAAGTACTGC TGCTGACTGA TGGGGAGGAT AACACTGCAA GTTCTTGTAT TGATGAAGTG 1320 AAACAAAGTG GGGCCATTGT TCATTTTATT GCTTTGGGAA GAGCTGCTGA TGAAGCAGTA 1380 ATAGAGATGA GCAAGATAAC AGGAGGAAGT CATTTTTATG TTTCAGATGA AGCTCAGAAC 1440 AATGGCCTCA TTGATGCTTT TGGGGCTCTT ACATCAGGAA ATACTGATCT CTCCCAGAAG 1500 TCCCTTCAGC TCGAAAGTAA GGGATTAACA CTGAATAGTA ATGCCTGGAT GAACGACACT 1560 GTCATAATTG ATAGTACAGT GGGAAAGGAC ACGTTCTTTC TCATCACATG GAACAGTCTG 1620 CCTCCCAGTA TTTCTCTCTG GGATCCCAGT GGAACAATAA TGGAAAATTT CACAGTGGAT 1680 GCAACTTCCA AAATGGCCTA TCTCAGTATT CCAGGAACTG CAAAGGTGGG CACTTGGGCA 1740 TACAATCTTC AAGCCAAAGC GAACCCAGAA ACATTAACTA TTACAGTAAC TTCTCGAGCA 1800 GCAAATTCTT CTGTGCCTCC AATCACAGTG AATGCTAAAA TGAATAAGGA CGTAAACAGT 1860 TTCCCCAGCC CAATGATTGT TTACGCAGAA ATTCTACAAG GATATGTACC TGTTCTTGGA 1920 GCCAATGTGA CTGCTTTCAT TGAATCACAG AATGGACATA CAGAAGTTTT GGAACTTTTG 1980 GATAATGGTG CAGGCGCTGA TTCTTTCAAG AATGATGGAG TCTACTCCAG GTATTTTACA 2040 GCATATACAG AAAATGGCAG ATATAGCTTA AAAGTTCGGG CTCATGGAGG AGCAAACACT 2100 GCCAGGCTAA AATTACGGCC TCCACTGAAT AGAGCCGCGT ACATACCAGG CTGGGTAGTG 2160 AACGGGGAAA TTGAAGCAAA CCCGCCAAGA CCTGAAATTG ATGAGGATAC TCAGACCACC 2220 TTGGAGGATT TCAGCCGAAC AGCATCCGGA GGTGCATTTG TGGTATCACA AGTCCCAAGC 2280 CTTCCCTTGC CTGACCAATA CCCACCAAGT CAAATCACAG ACCTTGATGC CACAGTTCAT 2340 GAGGATAAGA TTATTCTTAC ATGGACAGCA CCAGGAGATA ATTTTGATGT TGGAAAAGTT 2400 CAACGTTATA TCATAAGAAT AAGTGCAAGT ATTCTTGATC TAAGAGACAG TTTTGATGAT 2460 GCTCTTCAAG TAAATACTAC TGATCTGTCA CCAAAGGAGG CCAACTCCAA GGAAAGCTTT 2520 GCATTTAAAC CAGAAAATAT CTCAGAAGAA AATGCAACCC ACATATTTAT TGCCATTAAA 2580 AGTATAGATA AAAGCAATTT GACATCAAAA GTATCCAACA TTGCACAAGT AACTTTGTTT 2640 ATCCCTCAAG CAAATCCTGA TGACATFGAT CCTACTCCTA CTCCTACTCC TACTCCTGAT 2700 AAAAGTCATA ATTCTGGAGT TAATATTTCT ACGCTGGTAT TGTCTGTGAT TGGGTCTGTT 2760 GTAATTGTTA ACTTTATTTT AAGTACCACC ATTTGAACCT TAACGAAGAA AAAAATCTTC 2820 AAGTAGACCT AGAAGAGAGT TTTAAAAAAC AAAACAATGT AAGTAAAGGA TATTTCTGAA 2880 TCTTAAAATT CATCCCATGT GTGATCATAA ACTCATAAAA ATAATTTTAA GATGTCGGAA 2940 AAGGATACTT TGATTAAATA AAAACACTCA TGGATATGTA AAAACTGTCA AGATTAAAAT 3000 TTAATAGTTT CATTTATTTG TTATTTTATT TGTAAGAAAT AGTGATGAAC AAAGATCCTT 3060 TTTCATACTG ATACCTGGTT GTATATTATT TGATGCAACA GTTTTCTGAA ATGATATTTC 3120 AAATTGCATC AAGAAATTAA AATCATCTAT CTGAGTAGTC AAAATACAAG TAAAGGAGAG 3180 CAAATAAACA ACATTTGGAA AAAAAAAAAA AAAAAAAA Seq ID NO: 34 Protein sequence: Protein Accession #: NP_036260.1 1   11   21   31   41   51 |  |   |    |   |   | MGLFRGFVFL LVLCLLHQSN TSFIKLNNNG FEDIVIVIDP SVPEDEKIIE QIEDMVTTAS 60 TYLFEATEKR FFFKNVSILI PENWKENPQY KRPKHENHKH ADVIVAPPTL PGRDEPYTKQ 120 FTECGEKGEY IHFTPDLLLG KKQNEYGPPG KLFVHEWAHL RWGVFDEYNE DQPFYRAKSK 180 KIEATRCSAG ISGRNRVYKC QGGSCLSRAC RIDSTTKLYG KDCQFFPDKV QTEKASIMFM 240 QSIDSVVEFC NEKTHNQEAP SLQNIKCNFR STWEVISNSE DFKNTIPMVT PPPPPVFSLL 300 KIRQRIVCLV LDKSGSMGGK DRLNRMNQAA KHFLLQTVEN GSWVGMVHFD STATIVNKLI 360 QIKSSDERNT LMAGLPTYPL GGTSICSGIK YAFQVIGELH SQLDGSEVLL LTDGEDNTAS 420 SCIDEVKQSG AIVHFIALGR AADEAVIEMS KITGGSHFYV SDEAQNNGLI DAFGALTSGN 480 TDLSQKSLQL ESKGLTLNSN AWMNDTVIID STVGKDTFFL ITWNSLPPSI SLWDPSGTIM 540 ENFTVDATSK MAYLSIPGTA KVGTWAYNLQ AKANPETLTI TVTSRAANSS VPPITVNAKM 600 NKDVNSFPSP MIVYAEILQG YVPVLGANVT AFIESQNGHT EVLELLDNGA GADSFKNDGV 660 YSRYFTAYTE NGRYSLKVRA HGGANTARLK LRPPLNRAAY IPGWVVNGEI EANPPRPEID 720 EDTQTTLEDF SRTASGGAFV VSQVPSLPLP DQYPPSQITD LDATVHEDKI ILTWTAPGDN 780 FDVGKVQRYI IRISASILDL RDSFDDALQV NTTDLSPKEA NSKESFAFKP ENISEENATH 840 IFIAIKSIDK SNLTSKVSNI AQVTLFIPQA NPDDIDPTPT PTPTPDKSHN SGVNISTLVL 900 SVIGSVVIVN FILSTTI Seq ID NO: 35 DNA sequence Nucleic Acid Accession #: NM_000901.1 Coding sequence: 217-3171 1   11   21   31   41   51 |  |   |    |   |   | CGCGGGAGCC AACTTCAGGC TGCTCAGAGG AAGCCCGTGC AGTCAGTCAC CTGGGTGCAA 60 GAGCGTTGCT GCCTCGGGCT CTCCCGCTGC AGGGAGAGCG GCACTCGCTG GCCTGGATGT 120 GGTTGGATTT AGGGGGGCTC CGCAGCAGGG GTTTCGTGGC GGTGGCAAGC GCTGCAACAG 180 GTAGACGGCG AGAGACGGAC CCCGGCCGAG GCAGGGATGG AGACCAAAGG CTACCACAGT 240 CTCCCTGAAG GTCTAGATAT GGAAAGACGG TGGGGTCAAG TTTCTCAGGC TGTGGAGCGT 300 TCTTCCCTGG GACCTACAGA GAGGACCGAT GAGAATAACT ACATGGAGAT TGTCAACGTA 360 AGCTGTGTTT CCGGTGCTAT TCCAAACAAC AGTACTCAAG GAAGCAGCAA AGAAAAACAA 420 GAACTACTCC CTTGCCTTCA GCAAGACAAT AATCGGCCTG GGATTTTAAC ATCTGATATT 480 AAAACTGAGC TGGAATCTAA GGAACTTTCA GCAACTGTAG CTGAGTCCAT GGGTTTATAT 540 ATGGATTCTG TAAGAGATGC TGACTATTCC TATGAGCAGC AGAACCAACA AGGAAGCATG 600 AGTCCAGCTA AGATTTATCA GAATGTTGAA CAGCTGGTGA AATTTTACAA AGGAAATGGC 660 CATCGTCCTT CCACTCTAAG TTGTGTGAAC ACGCCCTTGA GATCATTTAT GTCTGACTCT 720 GGGAGCTCCG TGAATGGTGG CGTCATGCGC GCCATTGTTA AAAGCCCTAT CATGTGTCAT 780 GAGAAAAGCC CGTCTGTTTG CAGCCCTCTG AACATGACAT CTTCGGTTTG CAGCCCTGCT 840 GGAATCAACT CTGTGTCCTC CACCACAGCC AGCTTTGGCA GTTTTCCAGT GCACAGCCCA 900 ATCACCCAGG GAACTCCTCT GACATGCTCC CCTAATGCTG AAAATCGAGG CTCCAGGTCG 960 CACAGCCCTG CACATGCTAG CAATGTGGGC TCTCCTCTCT CAAGTCCGTT AAGTAGCATG 1020 AAATCCTCAA TTTCCAGCCC TCCAAGTCAC TGCAGTGTAA AATCTCCAGT CTCCAGTCCC 1080 AATAATGTCA CTCTGAGATC CTCTGTGTCT AGCCCTGCAA ATATTAACAA CTCAAGGTGC 1140 TCTGTTTCCA GCCCTTCGAA CACTAATAAC AGATCCACGC TTTCCAGTCC GGCAGCCAGT 1200 ACTGTGGGAT CTATCTGTAG CCCTGTAAAC AATGCCTTCA GCTACACTGC TTCTGGCACC 1260 TCTGCTGGAT CCAGTACATT GCGGGATGTG GTTCCCAGTC CAGACACGCA GGAGAAAGGT 1320 GCTCAAGAGG TCCCTTTTCC TAAGACTGAG GAAGTAGAGA GTGCCATCTC AAATGGTGTG 1380 ACTGGCCAGC TTAATATTGT CCAGTACATA AAACCAGAAC CAGATGGAGC TTTTAGCAGC 1440 TCATGTCTAG GAGGAAATAG CAAAATAAAT TCGGATTCTT CATTCTCAGT ACCAATAAAG 1500 CAAGAATCAA CCAAGCATTC ATGTTCAGGC ACCTCTTTTA AAGGGAATCC AACAGTAAAC 1560 CCGTTTCCAT TTATGGATGG CTCGTATTTT TCCTTTATGG ATGATAAAGA CTATTATTCC 1620 CTATCAGGAA TTTTAGGACC ACCTGTGCCC GGCTTTGATG GTAACTGTGA AGGCAGCGGA 1680 TTCCCAGTGG GTATTAAACA AGAACCAGAT GACGGGAGCT ATTACCCAGA GGCCAGCATC 1740 CCTTCCTCTG CTATTGTTGG GGTGAATTCA GGTGGACAGT CCTTCCACTA CAGGATTGGT 1800 GCTCAAGGTA CAATATCTTT ATCACGATCG GCTAGAGACC AATCTTTCCA ACACCTGAGT 1860 TCCTTTCCTC CTGTCAATAC TTTAGTGGAG TCATGGAAAT CACACGGCGA CCTGTCGTCT 1920 AGAAGAAGTG ATGGGTATCC GGTCTTAGAA TACATTCCAG AAAATGTATC AAGCTCTACT 1980 TTACGAAGTG TTTCTACTGG ATCTTCAAGA CCTTCAAAAA TATGTTTGGT GTGTGGGGAT 2040 GAGGCTTCAG GATGCCATTA TGGGGTAGTC ACCTGTGGCA GCTGCAAAGT TTTCTTCAAA 2100 AGAGCAGTGG AAGGGCAACA CAACTATTTA TGTGCTGGAA GAAATGATTG CATCATTGAT 2160 AAGATTCGAC GAAAGAATTG TCCTGCTTGC AGACTTCAGA AATGTCTTCA AGCTGGAATG 2220 AATTTAGGAG CACGAAAGTC AAAGAAGTTG GGAAAGTTAA AAGGGATTCA CGAGGAGCAG 2280 CCACAGCAGC AGCAGCCCCC ACCCCCACCC CCACCCCCGC AAAGCCCAGA GGAAGGGACA 2340 ACGTACATCG CTCCTGCAAA AGAACCCTCG GTCAACACAG CACTGGTTCC TCAGCTCTCC 2400 ACAATCTCAC GAGCGCTCAC ACCTTCCCCC GTTATGGTCC TTGAAAACAT TGAACCTGAA 2460 ATTGTATATG CAGGCTATGA CAGCTCAAAA CCAGATACAG CCGAAAATCT GCTCTCCACG 2520 CTCAACCGCT TAGCAGGCAA ACAGATGATC CAAGTCGTGA AGTGGGCAAA GGTACTTCCA 2580 GGATTTAAAA ACTTGCCTCT TGAGGACCAA ATTACCCTAA TCCAGTATTC TTGGATGTGT 2640 CTATCATCAT TTGCCTTGAG CTGGAGATCG TACAAACATA CGAACAGCCA ATTTCTCTAT 2700 TTTGCACCAG ACCTAGTCTT TAATGAAGAG AAGATGCATC AGTCTGCCAT GTATGAACTA 2760 TGCCAGGGGA TGCACCAAAT CAGCCTTCAG TTCGTTCGAC TGCAGCTCAC CTTTGAAGAA 2820 TACACCATCA TGAAAGTTTT GCTGCTACTA AGCACAATTC CAAAGGATGG CCTCAAAAGC 2880 CAGGCTGCAT TTGAAGAAAT GAGGACAAAT TACATCAAAG AACTGAGGAA GATGGTAACT 2940 AAGTGTCCCA ACAATTCTGG GCAGAGCTGG CAGAGGTTCT ACCAACTGAC CAAGCTGCTG 3000 GACTCCATGC ATGACCTGGT GAGCGACCTG CTGGAATTCT GCTTCTACAC CTTCCGAGAG 3060 TCCCATGCGC TGAAGGTAGA GTTCCCCGCA ATGCTGGTGG AGATCATCAG CGACCAGCTG 3120 CCCAAGGTGG AGTCGGGGAA CGCCAAGCCG CTCTACTTCC ACCGGAAGTG ACTGCCCGCT 3180 GCCCAGAAGA ACTTTGCCTT AAGTTTCCCT GTGTTGTTCC ACACCCAGAA GGACCCAAGA 3240 AAACCTGTTT TTAACATGTG ATGGTTGATT CACACTTGTT CAACAGTTTC TCAAGTTTAA 3300 AGTCATGTCA GAGGTTTGGA GCCGGGAAAG CTGTTTTTCC GTGGATTTGG CGAGACCAGA 3360 GCAGTCTGAA GGATTCCCCA CCTCCAATCC CCCAGCGCTT AGAAACATGT TCCTGTTCCT 3420 CGGGATGAAA AGCCATATCT AGTCAATAAC TCTGATTTTG ATATTTTCAC AGATGGAAGA 3480 AGTTTTAACT ATGCCGTGTA GTTTCTGGTA TCGTTCGCTT GTTTTAAAAG GGTTCAAGGA 3540 CTAACGAACG TTTTAAAGCT TACCCTTGGT TTGCACATAA AACGTATAGT CAATATGGGG 3600 CATTAATATT CTTTTGTTAT TAAAAAAACA CAAAAAAATA ATAAAAAAAT ATATACAGAT 3660 TCCTGTTGTG TAATAACAGA ACTCGTGGCG TGGGGCAGCA GCTGCCTCTG AGCCCTCGCT 3720 CGTCCACGGT CTTCTGCATC ACTGGTATAC ACACTCGTTA GCGTCCATTT CTTATTTAAT 3780 TAGAATGGAT AAGATGATGT TAAATGCCTT GGTTTGATTT CTAGTATCTA TTGTGTTGGC 3840 TTTACAAATA ATTTTTTGCA GTCTTTTGCT GTGCTGTACA TTACTGTATG TATAAATTAT 3900 GAAGGACCTG AAATAAGGTA TAAGGATCTT TTGTAAATGA GACACATACA AAAAAAATCT 3960 TTAATGGTTA ATAGGATGAA TGGGAAAGTA TTTTTGAAAG AATTCTATTT TGCTGGAGAC 4020 TATTTAAGTA CTATCTTTGT CTAAACAAGG TAATTTTTTT TTGTAAAGTG CAATGTCCTG 4080 CATGCATAAT GAACCGTTTA CAGTGTATTT AAGAAAGGGA AAGCTGTGCC TTTTTTAGCT 4140 TCATATCTAA TTTACCATTA TTTTACAGTC TCTGTTGTAA ATAACCACAC TGAAACCTCT 4200 TCGGTTGTCT TGAAACCTTT CTACTTTTTC TGTACTTTTT GTTTTGTTCT TGGTCTCCCG 4260 CTTGGGGCAT TTGTGGGACT CCAGCACGTT TTCTGGCTTC TGCTTCATCC TGCTCCATCG 4320 GGGAATGACA CACTGCGGTG TCTGCAGCTC CTGGAAGGTG TCATTTGACA ACACATGTGG 4380 GAGAGGAGGT CCTTGGAGTG CTGCAGCTTT GGGAAAGCCT GCCTCGTTTC CCTTTTCCTC 4440 TAGAAGCAGA ACCAGCTCTA CGAGAGTGAG ACTGGGAACT TGATGGCTCA GAGAGCATCT 4500 TTTCCTCCCA TTTTAGAAAA TCAGATTTTC TCCTGTGGGA AAAAAAAATT CCATGCACTC 4560 TCTCTCTGTT AAAGATCAGC TATTCCCTTC TGATCTTGGA AAGAGGTTCT GCACTCCTGG 4620 AACCGGTCAC AGGAACGCAC AGATCATGGC AGGATGCGCT GGGACGGCCC ATCTTGGCAA 4680 GGTTCAGTCT GAATGGCATG GAGACCGGGA GATAGAGGGG TTTTAGATTT TTAAAAGGTA 4740 GGTTTTAAAA ATAAGTTTTA TACATAAACA GTTTTGGAGA AAAATTACAG ATCATATAAG 4800 CAAGACAGTG GCACTAAAAT GTTTAATTCA TTAATCTGTT TGTTTGGCAC TGATGCAATG 4860 TATGGCTTTT CTCTTGCCCC AAATCACAAA CATATGTATC TTTGGGGAAA CTAACAATAT 4920 GATTGCACTA AATAAACTAC TTTGAATAGA GGCCAAATTA ATCTTTTAAA AATGATGATA 4980 ATCATCAGGT TTACTCAGTG AAATCATATT AATTATTTTC CAAAATCTAA AAGCTGTAGC 5040 TGGAGAAGCC CATGGCCACG AGGAAGCAGC AATTAATTAG ATCAACACTT TTCTCCAGGG 5100 TTCACCATGC AGGCAACATT ACCTTGTCTT TCAAAAGACA CCTGCCTTAG TGCAAGGGGA 5160 AACCTGTGAA AGCTGCACTC AGAGGGAGGA GTCTTTCTTA CATAATTTGC AATTTCAGGA 5220 ATTTAATTTA TAGGCAGATC TTTAAATACA GTCAACTTAC GGTGCACAGT AATATGAAAG 5280 CCACACTTTG AAGGTAATAA ATACACAGCA TGCAGACTGG GAGTTGCTAG CAAACAAATG 5340 GCTTACTTAC AAAAGCAGCT TTTAGTTCAG ACTTAGTTTT TATAAAATGA GAATTCTGAC 5400 TTACTTAACC AGGTTTGGGA TGGAGATGGT CTGCATCAGC TTTTTGTATT AACAAAGTTA 5460 CTGGCTCTTT GTGTGTCTCC AGGTAACTTT GCTTGATTAA ACAGCAAAGC CATATTCTAA 5520 ATTCACTGTT GAATGCCTGT CCCAGTCCAA ATTGTCTGTC TGCTCTTATT TTTGTACCAT 5580 ATTGCTCTTA AAAATCTTGG TTTGGTACAG TTCATAATTC ACCAAAAAGT TCATATAATT 5640 TAAAGAAACA CTAAATTAGT TTAAAATGAA GCAATTTATA TCTTTATGCA AAAACATATG 5700 TCTGTCTTTG CAAAGGACTG TAAGCAGATT ACAATAAATC CTTTACTTT Seq ID NO: 36 Protein sequence: Protein Accession #: NP_000892.1 1   11   21   31   41   51 |  |   |    |   |   | METKGYHSLP EGLDMERRWG QVSQAVERSS LGPTERTDEN NYMEIVNVSC VSGAIPNNST 60 QGSSKEKQEL LPCLQQDNNR PGILTSDIKT ELESKELSAT VAESMGLYMD SVRDADYSYE 120 QQNQQGSMSP AKIYQNVEQL VKFYKGNGHR PSTLSCVNTP LRSFMSDSGS SVNGGVMRAI 180 VKSPIMCHEK SPSVCSPLNM TSSVCSPAGI NSVSSTTASF GSFPVHSPIT QGTPLTCSPN 240 AENRGSRSHS PAHASNVGSP LSSPLSSMKS SISSPPSHCS VKSPVSSPNN VTLRSSVSSP 300 ANINNSRCSV SSPSNTNNRS TKSSPAASTV GSICSPVNNA FSYTASGTSA GSSTLRDVVP 360 SPDTQEKGAQ EVPFPKTEEV ESAISNGVTG QLNIVQYIKP EPDGAFSSSC LGGNSKINSD 420 SSFSVPIKQE STKHSCSGTS FKGNPTVNPF PFMDGSYFSF MDDKDYYSLS GILGPPVPGF 480 DGNCEGSGFP VGIKQEPDDG SYYPEASIPS SAIVGVNSGG QSFHYRIGAQ GTISLSRSAR 540 DQSFQHLSSF PPVNTLVESW KSHGDLSSRR SDGYPVLEYI PENVSSSTLR SVSTGSSRPS 600 KICLVCGDEA SGCHYGVVTC GSCKVFFKRA VEGQHNYLCA GRNDCIIDKI RRKNCPACRL 660 QKCLQAGMNL GARKSKKLGK LKGIHEEQPQ QQQPPPPPPP PQSPEEGTTY IAPAKEPSVN 720 TALVPQLSTI SRALTPSPVM VLENIEPEIV YAGYDSSKPD TAENLLSTLN RLAGKQMIQV 780 VKWAKVLPGF KNLPLEDQIT LIQYSWMCLS SFALSWRSYK HTNSQFLYFA PDLVFNEEKM 840 HQSAMYELCQ GMHQISLQFV RLQLTFEEYT IMKVLLLLST IPKDGLKSQA AFEEMRTNYI 900 KELRKMVTKC PNNSGQSWQR FYQLTKLLDS MHDLVSDLLE FCFYTFRESH ALKVEFPAML 960 VEIISDQLPK VESGNAKPLY FHRK Seq ID NO: 37 DNA sequence Nucleic Acid Accession #: see Table 25 & 25A for complete list 1   11   21   31   41   51 |  |   |    |   |   | CCTACCAGGT TCAAGCAACT CTGCTGCCTC AGCTCCCAAG TAGCTGGGAT TACAGGTGCA 60 TGCCACTACA CCTGGCTTTT TGTATTTTTA GTAGAGATGG TTTTCACTAT GTTGGCCAGG 120 CTGATCTTGA ATTCCTGGCC TGAAGTAATC TGCCTGCCTC AGCCTCCCAA AGTGCTGGGA 180 TTATAGGAGC CACCACACCT GGCATAACTG GTATTTTTTA TATGCTTCCT GGGCAACTTA 240 AAAAATTGAT TACTCTGTTG TTTCTTCCTT TTTTTTTTTT TTTTGGCTTT GACCAATTTG 300 TGAGACCCAA GTATCTCCTA CCTAGAAAAA AAACACACTA AACAGTAAAT GATTACCAAC 360 CTATTTGGAA CAAATCTCAA TTAATTAACA TATACTTCAA GGAGAAGACT TAACAAAATC 420 TTACTTTTCA TTCTTAATAG CTCTTTCCAT AAAAATGTTC CACAAGTGTA TCAAATTAGT 480 CCTAACAACT ACTGTTAAGT GATTAATGAA ACAGGAGTGA CAGGAGTGAA TTTAATAATA 540 GCAATAAATA CAGATGGGAC TACATAAATT GTGGAGGTCC TGATGCAAAA CTCTCTCTGT 600 ATTCGATGGC ATCTCAGCTT TCTCATAGAG CTGTTTCACT GTGAGGGTCT TTATCCTTCA 660 TGCAGAGCTT CATTATTTTC TTTCTTCTAG CAATCAGTCC AAAGCACAAT GTCAGAAAGA 720 TCACAACACA TGCAGCAATA ATGGGCTCTA TTGGTACACC CACAGTTTTA TCTTTAACAA 780 TC Seq ID NO: 38 DNA sequence Nucleic Acid Accession #: NM_001192.1 Coding sequence: 219-773 1   11   21   31   41   51 |  |   |    |   |   | AAGACTCAAA CTTAGAAACT TGAATTAGAT GTGGTATTCA AATCCITACG TGCCGCGAAG 60 ACACAGACAG CCCCCGTAAG AACCCACGAA GCAGGCGAAG TTCATTGTTC TCAACATTCT 120 AGCTGCTCTT GCTGCATTTG CTCTGGAATT CTTGTAGAGA TATTACTTGT CCTTCCAGGC 180 TGTTCTTTCT GTAGCTCCCT TGT3TTCTTT TTGTGATCAT GTTGCAGATG GCTGGGCAGT 240 GCTCCCAAAA TGAATATTTT GACAGTTTGT TGCATGCTTG CATACCTTGT CAACTTCGAT 300 GTTCTTCTAA TACTCCTCCT CTAACATGTC AGCGTTATTG TAATGCAAGT GTGACCAATT 360 CAGTGAAAGG AACGAATGCG ATTCTCTGGA CCTGTTTGGG ACTGAGCTTA ATAATTTCTT 420 TGGCAGTITT CGTGCTAATG TTTTTGCTAA GGAAGATAAG CTCTGAACCA TTAAAGGACG 480 AGTTTAAAAA CACAGGATCA GGTCTCCTGG GCATGGCTAA CATTGACCTG GAAAAGAGCA 540 GGACTGGTGA TGAAATTATT CTTCCGAGAG GCCTCGAGTA CACGGTGGAA GAATGCACCT 600 GTGAAGACTG CATCAAGAGC AAACCGAAGG TCGACTCTGA CCATTGCTTT CCACTCCCAG 660 CTATGGAGGA AGGCGCAACC ATTCTTGTCA CCACGAAAAC GAATGACTAT TGCAAGAGCC 720 TGCCAGCTGC TTTGAGTGCT ACGGAGATAG AGAAATCAAT TTCTGCTAGG TAATTAACCA 780 TTTCGAcTCG AGCAGTGCCA CTTTAAAAAT CTTTTGTCAG AATAGATGAT GTGTCAGATC 840 TCTTTAGGAT GACTGTATTT TTCAGTTGCC GATACAGCTT TTTGTCCTCT AACTGTGGAA 900 ACTCTTTATG TTAGATATAT TTCTCTAGGT TACTGTTGGG AGCTTAATGG TAGAAACTTC 960 CTTGGTTTCA TGATTAAAGT CTTTTTTTTT CCTGA Seq ID NO: 39 Protein sequence: Protein Accession #: NP_001183.1 1   11   21   31   41   51 |  |   |    |   |   | MLQMAGQCSQ NEYFDSLLHA CIPCQLRCSS NTPPLTCQRY CNASVTNSVK GTNAILWTCL 60 GLSLIISLAV FVLMFLLRKI SSEPLKDEFK NTGSGLLGMA NIDLEKSRTG DEIILPRGLE 120 YTVEECTCED CIKSKPKVDS DHCFPLPAME EGATILVTTK TNDYCKSLPA ALSATEIEKS 180 ISAR Seq ID NO: 40 DNA sequence Nucleic Acid Accession #: NM_025087.1 Coding sequence: 183-2282 1   11   21   31   41   51 |  |   |    |   |   | ACACTGCCTC GGTFCGGCAA GTGGGTCAGT TGGCTGGGGC TCACTTGGCA ACGGGACGCG 60 GGAACGAGGG GCGCGGACGC AGGCCCGGGA GGACGCGGCG GCGGGAACCT GGGGGCGCAG 120 GGCTAGGGCA GCGGGCCCGA CCCGCACGGC TTTCCTGGAA AGCGCTGCCC CTCGCCGCGG 180 CGATGACCTC GCTGTGGAGA GAAATCCTCT TGGAGTCGCT GCTGGGATGT GTTTCTTGGT 240 CTCTCTACCA TGACCTGGGA CCGATGATCT ATTACTTTCC TTTGCAAACA CTAGAACTCA 300 CTGGGCTTGA AGGTTTTAGT ATAGCATTTC TTTCTCCAAT ATTCCTAACA ATTACTCCTT 360 TCTCGAAATT GGTTAACAAG AAGTGGATGC TAACCCTGCT GAGGATAATC ACTATTGGCA 420 GCATAGCCTC CTTCCAGGCT CCAAATGCCA AACTTCGACT GATGGTTCTT GCGCTTGGGG 480 TGTCTTCCTC ACTGATAGTG CAAGCTGTGA CTTGGTGGTC AGGAAGTCAT TTGCAAAGGT 540 ACCTCAGAAT TTGGGGATTC ATTTTAGGAC AGATTGTTCT TGTTGTTCTA CGCATATGGT 600 ATACTTCACT AAACCCAATC TGGAGTTATC AGATGTCCAA CAAAGTGATA CTGACATTAA 660 GTGCCATAGC CACACTTGAT CGTATTGGCA CAGATGGTGA CTGCAGTAAA CCTGAAGAAA 720 AGAAGACTGG TGAGGTAGCC ACGGGGATGG CCTCTAGACC CAACTGGCTG CTGGCAGGGG 780 CTGCTTTTGG TAGCCTTGTG TTCCTCACCC ACTGGGTTTT TGGAGAAGTC TCTCTTGTTT 840 CCAGATGGGC AGTGAGTGGG CATCCACATC CAGGGCCAGA TCCTAACCCA TTTGGAGGTG 900 CAGTACTGCT GTGCTTGGCA AGTGGATTGA TGCTTCCATC TTGTTTGTGG TTTCGTGGTA 960 CTGGTTTGAT CTGGTGGGTT ACAGGAACAG CTTCAGCTGC GGGGCTCCTT TACCTGCACA 1020 CATGGGCAGC TGCTGTGTCT GGCTGTGTCT TCGCCATCTT TACTGCATCC ATGTGGCCCC 1080 AAACACTTGG ACACCTTATT AACTCAGGGA CAAACCCTGG GAAAACCATG ACCATTGCCA 1140 TGATATTTTA TCTTCTAGAA ATATTTTTCT GTGCCTGGTG CACAGCTTTT AAGTTTGTCC 1200 CAGGAGGTGT CTACGCTAGA GAAAGATCAG ATGTGCTTTT GGGGACAATG ATGTTAATTA 1260 TCGGGCTGAA TATGCTATTT GGTCCTAAGA AAAACCTTGA TTTGCTTCTT CAAACAAAAA 1320 ACAGTTCTAA AGTGCYTTTC AGAAAGAGTG AAAAATACAT GAAACTTTTT CTGTGGCTGC 1380 TTGTTGGTGT GGGATTGTTG GGATTAGGAC TACGGCATAA AGCCTATGAG AGAAAACTGG 1440 GCAAAGTGGC ACCAACCAAA GAGGTCTCTG CTGCCATCTG GCCTTTCAGG TTTGGATATG 1500 ACAATGAAGG GTGGTCTAGT CTAGAAAGAT CAGCTCACCT GCTCAATGAA ACAGGTGCAG 1560 ATTTCATAAC AATTTTGGAG AGTGATGCTT CTAAGCCCTA TATGGGGAAC AATGACTTAA 1620 CCATGTGGCT AGGGGAAAAG TTGGGTTTCT ATACAGACTT TGGTCCAAGC ACAAGGTATC 1680 ACACTTGGGG GATTATGGCT TTGTCAAGAT ACCCAATTGT GAAATCTGAG CATCACCTTC 1740 TTCCGTCACC AGAGGGCGAG ATCGCACCAG CCATCACATT GACCGTTAAC ATTTCGGGCA 1800 AGCTGGTGGA TTTTGTCGTG ACACACTTTG GGAACCACGA AGATGACCTC GACAGGAAAC 1860 TGCAGGCTAT TGCTGTTTCA AAACTACTGA AAAGTAGCTC TAATCAAGTG ATATTTCTGG 1920 GATATATCAC TTCAGCACCT GGCTCCAGAG ATTATCTACA GCTCACTGAA CATGGCAATG 1980 TGAAGGATAT CGACAGCACT GATCATGACA GATGGTGTGA ATACATTATG TATCGAGGGC 2040 TGATCAGGTT GGGTTATGCA AGAATCTCCC ATGCTGAACT GAGTGATTCA GAAATTCAGA 2100 TGGCAAAATT TAGGATCCCT GATGACCCCA CTAATTATAG AGACAACCAG AAAGTGGTCA 2160 TAGACCACAG AGAAGTTTCT GAGAAAATTC ATTTTAATCC CAGATTTGGA TCCTACAAAG 2220 AAGGACACAA TTATGAAAAC AACCATAATT TTCATATGAA TACTCCCAAA TACTTTTTAT 2280 GAAACATTTA AAACAAGAAG TTATTGGCTG GGAAAATCTA AGAAAAAAAG TATGTAAGAT 2340 AAAAAGAAGA GATTAATGAA AGTGGGAAAA TACACATGAA GAACCTCAAC TTAAAAAACA 2400 CATGGTATCT ATGCAGTGGG AAATTACCTC CATTTGTAAA CTATGTTGCT TAATAAAAAC 2460 ATTTCTCTAA AAAAAAAAAA AAAAAA Seq ID NO: 41 Protein sequence: Protein Accession #: NP_079363.1 1   11   21   31   41   51 |  |   |    |   |   | MTSLWREILL ESLLGCVSWS LYHDLGPMIY YFPLQTLELT GLEGFSIAFL SPIFLTITPF 60 WKLVNKKWML TLLRIITIGS IASFQAPNAK LRLMVLALGV SSSLIVQAVT WWSGSHLQRY 120 LRIWGFILGQ IVLVVLRIWY TSLNPIWSYQ MSNKVILTLS AIATLDRIGT DGDCSKPEEK 180 KTGEVATGMA SRPNWLLAGA AFGSLVFLTH WVFGEVSLVS RWAVSGHPHP GPDPNPFGGA 240 VLLCLASGLM LPSCLWFRGT GLIWWVTGTA SAAGLLYLHT WAAAVSGCVF AIFTASMWPQ 300 TLGHLINSGT NPGKTMTIAM IFYLLEIFFC AWCTAFKFVP GGVYARERSD VLLGTMMLII 360 GLNMLFGPKK NLDLLLQTKN SSKVLFRKSE KYMKLFLWLL VGVGLLGLGL RHKAYERKLG 420 KVAPTKEVSA AIWPFRFGYD NEGWSSLERS AHLLNETGAD FITILESDAS KPYMGNNDLT 480 MWLGEKLGFY TDFGPSTRYH TWGIMALSRY PIVKSEHHLL PSPEGEIAPA ITLTVNISGK 540 LVDFVVTHFG NHEDDLDRKL QAIAVSKLLK SSSNQVIFLG YITSAPGSRD YLQLTEHGNV 600 KDIDSTDHDR WCEYIMYRGL IRLGYARISH AELSDSEIQM AKFRIPDDPT NYRDNQKVVI 660 DHREVSEKIH FNPRFGSYKE GHNYENNHNF HMNTPKYFL

[0362] It is understood that the examples described above in no way serve to limit the true scope of this invention, but rather are presented for illustrative purposes. All publication, sequences of accession numbers, and patent applications cited in this specification are herein incorporated by reference as if each individual publication or patent application were specifically and individually indicated to be incorporated by reference. 

What is claimed is:
 1. A method of detecting a metastatic colorectal cancer-associated transcript in a cell from a patient, the method comprising contacting a biological sample from the patient with a polynucleotide that selectively hybridizes to a sequence at least 80% identical to a sequence as shown in Tables 1-26.
 2. The method of claim 1, wherein the biological sample comprises isolated nucleic acids.
 3. The method of claim 1, wherein the polynucleotide is labeled.
 4. The method of claim 1, wherein the polynucleotide is immobilized on a solid surface.
 5. An isolated nucleic acid molecule consisting of a polynucleotide sequence as shown in Tables 1-26.
 6. An expression vector comprising the nucleic acid of claim
 5. 7. A host cell comprising the expression vector of claim
 6. 8. An isolated polypeptide which is encoded by a nucleic acid molecule having polynucleotide sequence as shown in Tables 1-26.
 9. An antibody that specifically binds a polypeptide of claim
 8. 10. The antibody of claim 10, which is an antibody fragment.
 11. The antibody of claim 10, which is a humanized antibody
 12. A method of detecting a metastatic colorectal cancer cell in a biological sample from a patient, the method comprising contacting the biological sample with an antibody of claim
 9. 13. The method of claim 12, wherein the antibody is labeled.
 14. A method of detecting antibodies specific to metastatic colorectal cancer in a patient, the method comprising contacting a biological sample from the patient with a polypeptide encoded by a nucleic acid comprises a sequence from Tables 1-26.
 15. A method for identifying a compound that modulates a metastatic colorectal cancer-associated polypeptide, the method comprising the steps of: (i) contacting the compound with a metastatic colorectal cancer-associated polypeptide, the polypeptide encoded by a polynucleotide that selectively hybridizes to a sequence at least 80% identical to a sequence as shown in Tables 1-26.; and (ii) determining the functional effect of the compound upon the polypeptide.
 16. The method of claim 15, wherein the functional effect is determined by measuring ligand binding to the polypeptide.
 17. A method of inhibiting proliferation of a metastatic colorectal cancer-associated cell to treat colorectal cancer in a patient, the method comprising the step of administering to the subject a therapeutically effective amount of a compound that modulates a polypeptide encoded by a sequence as shown in Tables 1-26.
 18. A drug screening assay comprising the steps of (i) administering a test compound to a mammal having colorectal cancer or a cell isolated therefrom; (ii) comparing the level of gene expression of a polynucleotide that selectively hybridizes to a sequence at least 80% identical to a sequence as shown in Tables 1-26. In a treated cell or mammal with the level of gene expression of the polynucleotide in a control cell or mammal, wherein a test compound that modulates the level of expression of the polynucleotide is a candidate for the treatment of colorectal cancer.
 19. A pharmaceutical composition for treating a mammal having colorectal cancer, the composition comprising a compound identified by the assay of claim 18 and a physiologically acceptable excipient.
 20. A method of detecting a metastatic colorectal cancer-associated polypeptide in a cell from a patient, the method comprising contacting a biological sample from the patient with a antibody that that specifically binds a polypeptide encoded by a nucleic acid molecule having polynucleotide sequence as shown in Tables 1-26.
 21. The method of claim 21, wherein the antibody is labeled. 